Name

symmetrical, oval parietal bone defects Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetrical, oval parietal bone defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; heart septal defects, atrial; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; heart septal defects, atrial; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symmetrical dyschromatosis of extremities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Symmetrical dyschromatosis of extremities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

multiple symmetrical lipomatosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease multiple symmetrical lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

symmetrical Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term symmetrical in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

peptidyl-arginine methylation, to symmetrical-dimethyl arginine Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-arginine methylation, to symmetrical-dimethyl arginine biological process from the curated GO Biological Process Annotations dataset.

bis(5'-nucleosyl)-tetraphosphatase (symmetrical) activity Gene Set

From GO Molecular Function Annotations

genes performing the bis(5'-nucleosyl)-tetraphosphatase (symmetrical) activity molecular function from the curated GO Molecular Function Annotations dataset.

symmetrical progressive peripheral demyelination Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetrical progressive peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital symmetrical palmoplantar keratosis Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital symmetrical palmoplantar keratosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Bed nuclei of the stria terminalis, anterior division, oval nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, oval nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

oval paracentral nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in oval paracentral nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

oval Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term oval in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

oval face Gene Set

From HPO Gene-Disease Associations

genes associated with the oval face phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal oval window morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal oval window morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal oval cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal oval cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent oval cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent oval cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal oval cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal oval cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormality of the parietal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the parietal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal parietal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal parietal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

parietal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the parietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged parietal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged parietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small parietal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small parietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent parietal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent parietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

bone resorption; fractures, bone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone resorption; fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; bone responsiveness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; bone responsiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low bone-mineral density and rapid postmenopausal bone loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low bone-mineral density and rapid postmenopausal bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

regulation of bone mineralization involved in bone maturation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of bone mineralization involved in bone maturation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of bone mineralization involved in bone maturation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations dataset.

bone mineralization involved in bone maturation Gene Set

From GO Biological Process Annotations

genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations dataset.

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Forebrain defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Forebrain defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart defects, multiple types, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heart Septal Defects, Ventricular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects, Ventricular from the curated CTD Gene-Disease Associations dataset.

Combined Cellular And Humoral Immune Defects With Granulomas Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.

Heart Septal Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects from the curated CTD Gene-Disease Associations dataset.

Neural Tube Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neural Tube Defects from the curated CTD Gene-Disease Associations dataset.

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Laterality Defects, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Laterality Defects, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Heart Septal Defects, Atrial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects, Atrial from the curated CTD Gene-Disease Associations dataset.

Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset.

Heart Defects, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Defects, Congenital from the curated CTD Gene-Disease Associations dataset.

Color Vision Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Color Vision Defects from the curated CTD Gene-Disease Associations dataset.

ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.

congenital heart defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft palate and calvaria defects. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft palate and calvaria defects. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; dihydropyrimidine dehydrogenase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; dihydropyrimidine dehydrogenase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dilatation, pathologic; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dilatation, pathologic; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathies; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathies; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

axial skeletal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease axial skeletal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left-right laterality defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left-right laterality defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects and preeclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects and preeclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

color vision defects; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, atrial; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, atrial; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; heart defects, congenital; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; heart defects, congenital; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ductus arteriosus, patent; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ductus arteriosus, patent; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

visual field defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease visual field defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, ventricular; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

defects Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term defects in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

defectsaffected Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term defectsaffected in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Conotruncal heart defects Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Conotruncal heart defects phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

progressive visual field defects Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive visual field defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lung segmentation defects Gene Set

From HPO Gene-Disease Associations

genes associated with the lung segmentation defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulmonary valve defects Gene Set

From HPO Gene-Disease Associations

genes associated with the pulmonary valve defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial respiratory chain defects Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial respiratory chain defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the hand bones Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

forearm reduction defects Gene Set

From HPO Gene-Disease Associations

genes associated with the forearm reduction defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

asymmetric, linear skin defects Gene Set

From HPO Gene-Disease Associations

genes associated with the asymmetric, linear skin defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Heart Septal Defects, Ventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects, Ventricular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Endocardial Cushion Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Endocardial Cushion Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Heart Defects, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Defects, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Color Vision Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Color Vision Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Heart Septal Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Heart Septal Defects, Atrial Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects, Atrial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Neural Tube Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neural Tube Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From OMIM Gene-Disease Associations

genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

{neural tube defects, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {neural tube defects, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

forebrain defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the forebrain defects phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, nonsyndromic, 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

{neural tube defects, folate-sensitive, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {neural tube defects, folate-sensitive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 1, with or without congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 1, with or without congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated OMIM Gene-Disease Associations dataset.

combined cellular and humoral immune defects with granulomas Gene Set

From OMIM Gene-Disease Associations

genes associated with the combined cellular and humoral immune defects with granulomas phenotype from the curated OMIM Gene-Disease Associations dataset.

neural tube defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the neural tube defects phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, congenital heart defects, and posterior embryotoxon Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 7, with or without av conduction defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, nonsyndromic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

pancreatic agenesis and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the pancreatic agenesis and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

Defects in cobalamin (B12) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in cobalamin (B12) metabolism pathway from the Reactome Pathways dataset.

Defects in vitamin and cofactor metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in vitamin and cofactor metabolism pathway from the Reactome Pathways dataset.

Defects in biotin (Btn) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in biotin (Btn) metabolism pathway from the Reactome Pathways dataset.

superior parietal lobule, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior parietal lobule, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulate gyrus, parietal part, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulate gyrus, parietal part, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulate gyrus, parietal part, left, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulate gyrus, parietal part, left, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior parietal lobule, left, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior parietal lobule, left, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior parietal lobule, left, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior parietal lobule, left, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulate gyrus, parietal part, left, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulate gyrus, parietal part, left, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

cingulate gyrus, parietal part, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cingulate gyrus, parietal part, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

superior parietal lobule, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in superior parietal lobule, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Posterior parietal association areas, layer 6a Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Posterior parietal association areas, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Posterior parietal association areas, layer 6b Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Posterior parietal association areas, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

parietal cortex Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in parietal cortex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Posterior parietal association areas, layer 4 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Posterior parietal association areas, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Posterior parietal association areas, layer 5 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Posterior parietal association areas, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Posterior parietal association areas Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Posterior parietal association areas relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Posterior parietal association areas, layer 2/3 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Posterior parietal association areas, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Posterior parietal association areas, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Posterior parietal association areas, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

posteroventral (inferior) parietal cortex_8 yrs_M_12841 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

parietal neocortex_9 pcw_M_12833 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in parietal neocortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_3 yrs_F_12836 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_10 mos_M_12977 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_37 yrs_M_12303 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_16 pcw_M_12879 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_12 pcw_F_13060 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_12 pcw_F_12960 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_4 mos_M_12296 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_16 pcw_M_12837 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_23 yrs_M_12300 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_13 pcw_M_12820 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_21 pcw_F_12365 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_36 yrs_M_12302 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_19 pcw_F_12885 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_16 pcw_M_12287 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_40 yrs_F_12304 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_13 pcw_M_12888 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_15 yrs_M_12299 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_13 pcw_F_12834 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_12 pcw_F_12835 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_4 yrs_M_12298 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in posteroventral (inferior) parietal cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

parietal neocortex_8 pcw_M_13058 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in parietal neocortex_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

posteroventral (inferior) parietal cortex_8 yrs_M_12841 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_3 yrs_F_12836 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

parietal neocortex_9 pcw_M_12833 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in parietal neocortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_19 yrs_F_12832 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_10 mos_M_12977 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_37 yrs_M_12303 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_16 pcw_M_12879 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_12 pcw_F_13060 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_11 yrs_F_12289 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_12 pcw_F_12960 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_37 pcw_M_263195015 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_23 yrs_M_12300 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_13 pcw_M_12820 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_13 pcw_M_12888 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_16 pcw_M_12837 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_19 pcw_F_12885 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_16 pcw_M_12287 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_40 yrs_F_12304 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_15 yrs_M_12299 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_4 mos_M_12890 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_13 pcw_F_12834 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_12 pcw_F_12835 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_36 yrs_M_12302 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

posteroventral (inferior) parietal cortex_8 yrs_M_12981 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in posteroventral (inferior) parietal cortex_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

parietal neocortex_8 pcw_M_13058 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in parietal neocortex_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

outer CP in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

SP in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in SP in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

SG in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in SG in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

SP in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in SP in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

VZ in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VZ in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

IZ in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in IZ in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer SZ in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer SZ in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

outer CP in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in outer CP in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

VZ in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VZ in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

IZ in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in IZ in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

VZ in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VZ in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

MZ in dorsomedial parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in MZ in dorsomedial parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

SP in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in SP in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

MZ in posterodorsal (superior) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in MZ in posterodorsal (superior) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

MZ in posteroventral (inferior) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in MZ in posteroventral (inferior) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

IZ in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in IZ in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Parietal foramina 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parietal foramina 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parietal foramina 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parietal foramina 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parietal Foramina 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parietal Foramina 3 from the curated CTD Gene-Disease Associations dataset.

Parietal Foramina 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parietal Foramina 2 from the curated CTD Gene-Disease Associations dataset.

Parietal Foramina Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parietal Foramina from the curated CTD Gene-Disease Associations dataset.

Parietal Foramina With Cleidocranial Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parietal Foramina With Cleidocranial Dysplasia from the curated CTD Gene-Disease Associations dataset.

Parietal Lobe Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Parietal Lobe in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

parietal lobe Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parietal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parietal Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term parietal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

glomerular parietal epithelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the glomerular parietal epithelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

glomerular parietal epithelial cell development Gene Set

From GO Biological Process Annotations

genes participating in the glomerular parietal epithelial cell development biological process from the curated GO Biological Process Annotations dataset.

parietal foramina Gene Set

From HPO Gene-Disease Associations

genes associated with the parietal foramina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia cutis congenita over posterior parietal area Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia cutis congenita over posterior parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

parietal bossing Gene Set

From HPO Gene-Disease Associations

genes associated with the parietal bossing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia cutis congenita over parietal area Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia cutis congenita over parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal gastric parietal cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal gastric parietal cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal parietal endoderm morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal parietal endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal parietal lobe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal parietal lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal glomerular capsule parietal layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal glomerular capsule parietal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal parietal yolk sac morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal parietal yolk sac morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

parietal capsular epithelium metaplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the parietal capsular epithelium metaplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

overlapping parietal bones Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the overlapping parietal bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent parietal endoderm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent parietal endoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

parietal foramina 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parietal foramina 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

parietal foramina 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parietal foramina 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

parietal foramina with cleidocranial dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the parietal foramina with cleidocranial dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

parietal lobe Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue parietal lobe in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

parietal trophoblast giant cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue parietal trophoblast giant cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

parietal lobe Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue parietal lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

parietal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue parietal ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Secretion of Hydrochloric Acid in Parietal Cells(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Secretion of Hydrochloric Acid in Parietal Cells(Homo sapiens) pathway from the Wikipathways Pathways dataset.

regulators of bone mineralization Gene Set

From Biocarta Pathways

proteins participating in the regulators of bone mineralization pathway from the Biocarta Pathways dataset.

bone remodeling Gene Set

From Biocarta Pathways

proteins participating in the bone remodeling pathway from the Biocarta Pathways dataset.

bone Gene Set

From BioGPS Mouse Cell Type and Tissue Gene Expression Profiles

genes with high or low expression in bone relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.

Autosomal recessive hypophosphatemic bone disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive hypophosphatemic bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gracile bone dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gracile bone dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasemia with bone disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasemia with bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bone fragility with contractures, arterial rupture, and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bone marrow failure syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bone marrow failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bone marrow failure, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bone marrow failure, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bent bone dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bent bone dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta type 2, thin-bone Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type 2, thin-bone phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

High bone mass Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the High bone mass phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bone Marrow Neoplasms Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Marrow Neoplasms from the curated CTD Gene-Disease Associations dataset.

Bone Marrow Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Marrow Diseases from the curated CTD Gene-Disease Associations dataset.

Bone Diseases, Metabolic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Diseases, Metabolic from the curated CTD Gene-Disease Associations dataset.

Bone Diseases, Developmental Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Diseases, Developmental from the curated CTD Gene-Disease Associations dataset.

Bone Cysts, Aneurysmal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Cysts, Aneurysmal from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 2 from the curated CTD Gene-Disease Associations dataset.

Giant Cell Tumor of Bone Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Giant Cell Tumor of Bone from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 3 from the curated CTD Gene-Disease Associations dataset.

Bone Diseases, Endocrine Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Diseases, Endocrine from the curated CTD Gene-Disease Associations dataset.

Fractures, Bone Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fractures, Bone from the curated CTD Gene-Disease Associations dataset.

Bone Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Diseases from the curated CTD Gene-Disease Associations dataset.

Bone Resorption Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Resorption from the curated CTD Gene-Disease Associations dataset.

Paget Disease Of Bone 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paget Disease Of Bone 4 from the curated CTD Gene-Disease Associations dataset.

Neoplasms, Bone Tissue Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neoplasms, Bone Tissue from the curated CTD Gene-Disease Associations dataset.

Fibrous Dysplasia of Bone Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrous Dysplasia of Bone from the curated CTD Gene-Disease Associations dataset.

Bone Neoplasms Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Neoplasms from the curated CTD Gene-Disease Associations dataset.

BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15 from the curated CTD Gene-Disease Associations dataset.

Bone Marrow failure syndromes Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Marrow failure syndromes from the curated CTD Gene-Disease Associations dataset.

Bone Fragility with Contractures, Arterial Rupture, and Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bone Fragility with Contractures, Arterial Rupture, and Deafness from the curated CTD Gene-Disease Associations dataset.

Alveolar Bone Loss Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alveolar Bone Loss from the curated CTD Gene-Disease Associations dataset.

Split-hand/foot malformation with long bone deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-hand/foot malformation with long bone deficiency from the curated CTD Gene-Disease Associations dataset.

Bone Density Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Bone Density in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

bone remodeling disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease bone remodeling disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone marrow disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease bone marrow disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone marrow cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease bone marrow cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone development disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease bone development disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

sost-related sclerosing bone dysplasia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease sost-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

paget's disease of bone Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease paget's disease of bone from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ischemic bone disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease ischemic bone disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease bone disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone resorption disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease bone resorption disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone inflammation disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease bone inflammation disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease bone cancer from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bone marrow cancer Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease bone marrow cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

paget's disease of bone Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease paget's disease of bone in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

bone remodeling disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease bone remodeling disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

ischemic bone disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease ischemic bone disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

bone resorption disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease bone resorption disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

bone disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease bone disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

bone structure disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease bone structure disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

bone inflammation disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease bone inflammation disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

bone cancer Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease bone cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

bone osteosarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone marrow cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone marrow cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone deterioration disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone deterioration disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ischemic bone disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease ischemic bone disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone resorption disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone resorption disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone giant cell tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone giant cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

long bone adamantinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease long bone adamantinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone inflammation disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone inflammation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone remodeling disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone remodeling disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone marrow disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone marrow disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone ewing's sarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone ewing's sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone development disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone development disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone epithelioid hemangioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone epithelioid hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone structure disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone structure disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

sost-related sclerosing bone dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sost-related sclerosing bone dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

malignant fibrous histiocytoma of bone Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease malignant fibrous histiocytoma of bone in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone benign neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

paget's disease of bone Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease paget's disease of bone in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone giant cell sarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone giant cell sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

fibrosarcoma of bone Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease fibrosarcoma of bone in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bone cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxia; bone necrosis; femur head necrosis; osteonecrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; bone necrosis; femur head necrosis; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone marrow diseases; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone marrow diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hip bone loss and fracture Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hip bone loss and fracture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone marrow diseases; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone marrow diseases; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; hearing loss; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; hearing loss; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

calcium homeostasis and peripheral bone density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease calcium homeostasis and peripheral bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early postmenopausal bone loss at the spine. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early postmenopausal bone loss at the spine. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontal attachment loss; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontitis; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal bone mineral density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; rett syndrome; scoliosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; rett syndrome; scoliosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; fractures, vertebral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fractures, vertebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases, metabolic; scoliosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases, metabolic; scoliosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; muscle strength Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; muscle strength in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; osteopenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; osteopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; bone diseases; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; bone diseases; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone marrow diseases; dyskeratosis congenita; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone marrow diseases; dyskeratosis congenita; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone necrosis; osteonecrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone necrosis; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

paget's disease of bone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease paget's disease of bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis, postmenopausal; bone density; hormone disturbance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis, postmenopausal; bone density; hormone disturbance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; fractures, bone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; chronic periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; chronic periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mineralization Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineralization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone size Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early marginal bone loss around endosseous dental implants. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early marginal bone loss around endosseous dental implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; rett syndrome; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density but not spondylosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density but not spondylosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; bone mineral density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

primary bone lymphomas. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease primary bone lymphomas. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone necrosis; femur head necrosis; osteonecrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone necrosis; femur head necrosis; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone resorption; calcinosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone resorption; calcinosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft-versus-host disease; bone marrow transplantation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft-versus-host disease; bone marrow transplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mineral density (bmd) / quantitative ultra sound (qus) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density (bmd) / quantitative ultra sound (qus) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; fracture risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fracture risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; bone necrosis; liver cirrhosis; osteonecrosis; pancreatitis, alcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; bone necrosis; liver cirrhosis; osteonecrosis; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone necrosis; lupus erythematosus, systemic; osteonecrosis; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone necrosis; lupus erythematosus, systemic; osteonecrosis; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoarthritis; osteoarthritis, knee Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoarthritis; osteoarthritis, knee in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases, developmental; osteoarthritis, hip Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases, developmental; osteoarthritis, hip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone marrow diseases; dyskeratosis congenita Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone marrow diseases; dyskeratosis congenita in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

combined bone mass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease combined bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone cancer; soft tissue sarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone cancer; soft tissue sarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontal attachment loss; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontal attachment loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone phenotypes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone phenotypes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; sarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; sarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporosis; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporosis; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mineral density (spine) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density (spine) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone marrow transplant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone marrow transplant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone resorption; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone resorption; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases, metabolic; osteoporosis; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases, metabolic; osteoporosis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases, metabolic; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases, metabolic; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrous dysplasia of bone; osteitis fibrosa disseminata; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrous dysplasia of bone; osteitis fibrosa disseminata; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; neoplasm invasiveness; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; neoplasm invasiveness; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyotrophic lateral sclerosis; bone resorption; lead poisoning Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis; bone resorption; lead poisoning in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; spondylosis, lumbar Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; spondylosis, lumbar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; arthritis, rheumatoid; rheumatoid arthritis; sjogren's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; arthritis, rheumatoid; rheumatoid arthritis; sjogren's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; bone density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone resorption; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone resorption; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mineral density (bmd) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density (bmd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

very low bone mass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease very low bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone necrosis; osteonecrosis; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone necrosis; osteonecrosis; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early marginal bone loss around endosseous implants. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early marginal bone loss around endosseous implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density and spondylosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density and spondylosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone resorption; vitamin k deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone resorption; vitamin k deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases; degenerative arthropathy ; osteoarthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases; degenerative arthropathy ; osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone necrosis; jaw diseases; neuralgia; osteonecrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone necrosis; jaw diseases; neuralgia; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; fractures; osteocalcin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fractures; osteocalcin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; calcium; fractures, nonvertebral; milk intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; calcium; fractures, nonvertebral; milk intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density dehydroepiandrosterone sulphate osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density dehydroepiandrosterone sulphate osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cushing syndrome; fractures, bone; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cushing syndrome; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone resorption Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone resorption in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone marrow transplantation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone marrow transplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; height Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; fractures, closed; humeral fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; fractures, closed; humeral fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; gram-negative bacterial infections; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; gram-negative bacterial infections; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases, metabolic; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases, metabolic; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

decreased bone mass in patients Gene Set

From GAD Gene-Disease Associations

genes associated with the disease decreased bone mass in patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; gastrointestinal diseases; hematologic diseases; kidney diseases; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; gastrointestinal diseases; hematologic diseases; kidney diseases; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; bone diseases, metabolic; osteoporosis; thalassemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; bone diseases, metabolic; osteoporosis; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; dental fistula; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; dental fistula; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

paget disease of bone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease paget disease of bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; bone necrosis; osteonecrosis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; bone necrosis; osteonecrosis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mass; osteoporotic fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mass; osteoporotic fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone metastases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone metastases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; bone resorption; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; bone resorption; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus; dyslipidemias; fractures, bone; hypertension; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus; dyslipidemias; fractures, bone; hypertension; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammatory bowel disease; bone density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammatory bowel disease; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; coronary calcification Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; coronary calcification in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; hip fractures; osteoporosis; spinal injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; hip fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; tricho-dento-osseous syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; tricho-dento-osseous syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mineral density (hip) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density (hip) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

testosterone; bone density; stature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease testosterone; bone density; stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mineral density ; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density ; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone marrow diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone marrow diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis, postmenopausal; bone density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis, postmenopausal; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone characteristics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone characteristics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

peak bone mass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease peak bone mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mineral density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hip bone size Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hip bone size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mineral mass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporotic fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporotic fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; height; pth; pyridinoline, urinary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; height; pth; pyridinoline, urinary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; fractures, bone; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia ; bone mineral density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia ; bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term bone in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

TET2_KO_GDS4287_429_mouse_LSK - bone marrow progenitor population Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the TET2_KO_GDS4287_429_mouse_LSK - bone marrow progenitor population gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

RUNX2_NULL MUTATION_GDS2184_719_mouse_Embryonal bone (MG-U74A) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the RUNX2_NULL MUTATION_GDS2184_719_mouse_Embryonal bone (MG-U74A) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

TET2_KO_GDS4287_430_mouse_CMP - bone marrow progenitor population Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the TET2_KO_GDS4287_430_mouse_CMP - bone marrow progenitor population gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

TET2_KO_GDS4287_431_mouse_GMP - bone marrow progenitor population Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the TET2_KO_GDS4287_431_mouse_GMP - bone marrow progenitor population gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

negative regulation of bone remodeling Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of bone remodeling biological process from the curated GO Biological Process Annotations dataset.

ossification involved in bone remodeling Gene Set

From GO Biological Process Annotations

genes participating in the ossification involved in bone remodeling biological process from the curated GO Biological Process Annotations dataset.

positive regulation of bone resorption Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of bone resorption biological process from the curated GO Biological Process Annotations dataset.

cell proliferation in bone marrow Gene Set

From GO Biological Process Annotations

genes participating in the cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations dataset.

hematopoietic stem cell migration to bone marrow Gene Set

From GO Biological Process Annotations

genes participating in the hematopoietic stem cell migration to bone marrow biological process from the curated GO Biological Process Annotations dataset.

semaphorin-plexin signaling pathway involved in bone trabecula morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the semaphorin-plexin signaling pathway involved in bone trabecula morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of apoptotic process in bone marrow Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of apoptotic process in bone marrow biological process from the curated GO Biological Process Annotations dataset.

fibroblast growth factor receptor signaling pathway involved in negative regulation of apoptotic process in bone marrow Gene Set

From GO Biological Process Annotations

genes participating in the fibroblast growth factor receptor signaling pathway involved in negative regulation of apoptotic process in bone marrow biological process from the curated GO Biological Process Annotations dataset.

chondrocyte morphogenesis involved in endochondral bone morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the chondrocyte morphogenesis involved in endochondral bone morphogenesis biological process from the curated GO Biological Process Annotations dataset.

endochondral bone growth Gene Set

From GO Biological Process Annotations

genes participating in the endochondral bone growth biological process from the curated GO Biological Process Annotations dataset.

positive regulation of bone development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of bone development biological process from the curated GO Biological Process Annotations dataset.

fibroblast growth factor receptor signaling pathway involved in positive regulation of cell proliferation in bone marrow Gene Set

From GO Biological Process Annotations

genes participating in the fibroblast growth factor receptor signaling pathway involved in positive regulation of cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations dataset.

negative regulation of bone mineralization Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of bone mineralization biological process from the curated GO Biological Process Annotations dataset.

chondrocyte development involved in endochondral bone morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the chondrocyte development involved in endochondral bone morphogenesis biological process from the curated GO Biological Process Annotations dataset.

bone mineralization Gene Set

From GO Biological Process Annotations

genes participating in the bone mineralization biological process from the curated GO Biological Process Annotations dataset.

negative regulation of bone development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of bone development biological process from the curated GO Biological Process Annotations dataset.

bone trabecula morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the bone trabecula morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of apoptotic process in bone marrow Gene Set

From GO Biological Process Annotations

genes participating in the regulation of apoptotic process in bone marrow biological process from the curated GO Biological Process Annotations dataset.

regulation of bone mineralization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of bone mineralization biological process from the curated GO Biological Process Annotations dataset.

regulation of bone remodeling Gene Set

From GO Biological Process Annotations

genes participating in the regulation of bone remodeling biological process from the curated GO Biological Process Annotations dataset.

negative regulation of bone resorption Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of bone resorption biological process from the curated GO Biological Process Annotations dataset.

bone maturation Gene Set

From GO Biological Process Annotations

genes participating in the bone maturation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of bone trabecula formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of bone trabecula formation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of bone remodeling Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of bone remodeling biological process from the curated GO Biological Process Annotations dataset.

bone development Gene Set

From GO Biological Process Annotations

genes participating in the bone development biological process from the curated GO Biological Process Annotations dataset.

apoptotic process in bone marrow Gene Set

From GO Biological Process Annotations

genes participating in the apoptotic process in bone marrow biological process from the curated GO Biological Process Annotations dataset.

bone remodeling Gene Set

From GO Biological Process Annotations

genes participating in the bone remodeling biological process from the curated GO Biological Process Annotations dataset.

bone resorption Gene Set

From GO Biological Process Annotations

genes participating in the bone resorption biological process from the curated GO Biological Process Annotations dataset.

regulation of bone trabecula formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of bone trabecula formation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of bone mineralization Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of bone mineralization biological process from the curated GO Biological Process Annotations dataset.

regulation of bone resorption Gene Set

From GO Biological Process Annotations

genes participating in the regulation of bone resorption biological process from the curated GO Biological Process Annotations dataset.

ossification involved in bone maturation Gene Set

From GO Biological Process Annotations

genes participating in the ossification involved in bone maturation biological process from the curated GO Biological Process Annotations dataset.

bone marrow development Gene Set

From GO Biological Process Annotations

genes participating in the bone marrow development biological process from the curated GO Biological Process Annotations dataset.

regulation of cell proliferation in bone marrow Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations dataset.

bone trabecula formation Gene Set

From GO Biological Process Annotations

genes participating in the bone trabecula formation biological process from the curated GO Biological Process Annotations dataset.

cartilage development involved in endochondral bone morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cartilage development involved in endochondral bone morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of bone development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of bone development biological process from the curated GO Biological Process Annotations dataset.

bone morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the bone morphogenesis biological process from the curated GO Biological Process Annotations dataset.

endochondral bone morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the endochondral bone morphogenesis biological process from the curated GO Biological Process Annotations dataset.

chondrocyte differentiation involved in endochondral bone morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the chondrocyte differentiation involved in endochondral bone morphogenesis biological process from the curated GO Biological Process Annotations dataset.

bone cell development Gene Set

From GO Biological Process Annotations

genes participating in the bone cell development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cell proliferation in bone marrow Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations dataset.

structural constituent of bone Gene Set

From GO Molecular Function Annotations

genes performing the structural constituent of bone molecular function from the curated GO Molecular Function Annotations dataset.

Femoral neck bone geometry Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Femoral neck bone geometry phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hip bone size Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hip bone size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (paediatric, upper limb) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, upper limb) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (hip) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (hip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (paediatric, total body less head) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, total body less head) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (paediatric, skull) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, skull) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Femoral neck bone geometry and menarche (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Femoral neck bone geometry and menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Spine bone size Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Spine bone size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (paediatric, lower limb) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, lower limb) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone properties (heel) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone properties (heel) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (spine) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (spine) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

bone remodeling disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease bone remodeling disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

bone marrow disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease bone marrow disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

bone marrow cancer Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease bone marrow cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

bone development disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease bone development disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

paget's disease of bone Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease paget's disease of bone in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

ischemic bone disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease ischemic bone disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

bone resorption disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease bone resorption disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

bone deterioration disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease bone deterioration disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

bone disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease bone disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

bone structure disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease bone structure disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

bone inflammation disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease bone inflammation disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

bone cancer Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease bone cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

abnormality of forearm bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of forearm bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of upper limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

reduced bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the reduced bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of long bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hip bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal bone structure Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal bone structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

patchy changes of bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the patchy changes of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal cortical bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

sclerosis of hand bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sclerosis of hand bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

sclerosis of foot bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sclerosis of foot bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

increased bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the increased bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of bone marrow cell morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of pelvic girdle bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lower limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limb bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

bone marrow Gene Set

From HPA Tissue Gene Expression Profiles

genes with high or low expression in bone marrow relative to other tissues from the HPA Tissue Gene Expression Profiles dataset.

bone marrow Gene Set

From HPA Tissue Protein Expression Profiles

proteins with high or low expression in bone marrow relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.

increased bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the increased bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal bone structure Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal bone structure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of lower limb bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of lower limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of forearm bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of upper limb bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patchy changes of bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy changes of bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

malaligned carpal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the malaligned carpal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dumbbell-shaped long bone Gene Set

From HPO Gene-Disease Associations

genes associated with the dumbbell-shaped long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the nasal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized bone demineralization Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized bone demineralization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cortical bone morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal cortical bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal trabecular bone morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal trabecular bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cortical thickening of long bone diaphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the cortical thickening of long bone diaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of limb bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

rough bone trabeculation Gene Set

From HPO Gene-Disease Associations

genes associated with the rough bone trabeculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sparse bone trabeculae Gene Set

From HPO Gene-Disease Associations

genes associated with the sparse bone trabeculae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of long bone morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of long bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

megaloblastic bone marrow Gene Set

From HPO Gene-Disease Associations

genes associated with the megaloblastic bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the nasal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

marked delay in bone age Gene Set

From HPO Gene-Disease Associations

genes associated with the marked delay in bone age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of carpal bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of carpal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dysharmonic bone age Gene Set

From HPO Gene-Disease Associations

genes associated with the dysharmonic bone age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the capitate bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the capitate bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

carpal bone hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the carpal bone hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the hip bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the hip bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skin dimple over apex of long bone angulation Gene Set

From HPO Gene-Disease Associations

genes associated with the skin dimple over apex of long bone angulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pelvis bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pelvis bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent forearm bone Gene Set

From HPO Gene-Disease Associations

genes associated with the absent forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal ossification of the pubic bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal ossification of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the temporal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the temporal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the hamate bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the hamate bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bone-marrow foam cells Gene Set

From HPO Gene-Disease Associations

genes associated with the bone-marrow foam cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of pelvic girdle bone morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of pelvic girdle bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

frontal bone hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the frontal bone hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal bone collagen fibril morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal bone collagen fibril morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

carpal bone aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the carpal bone aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

delayed pubic bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the delayed pubic bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased density of long bone diaphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the increased density of long bone diaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bone cyst Gene Set

From HPO Gene-Disease Associations

genes associated with the bone cyst phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

slender long bone Gene Set

From HPO Gene-Disease Associations

genes associated with the slender long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nasal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplastic pubic bone Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplastic pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal morphology of forearm bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal morphology of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of multiple cell lineages in the bone marrow Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of multiple cell lineages in the bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the first metatarsal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the first metatarsal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sclerosis of foot bone Gene Set

From HPO Gene-Disease Associations

genes associated with the sclerosis of foot bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the fifth metatarsal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the fifth metatarsal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cystic angiomatosis of bone Gene Set

From HPO Gene-Disease Associations

genes associated with the cystic angiomatosis of bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

endopolyploidy on chromosome studies of bone marrow Gene Set

From HPO Gene-Disease Associations

genes associated with the endopolyploidy on chromosome studies of bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reduced bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the fourth metatarsal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the fourth metatarsal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

accelerated bone age after puberty Gene Set

From HPO Gene-Disease Associations

genes associated with the accelerated bone age after puberty phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short long bone Gene Set

From HPO Gene-Disease Associations

genes associated with the short long bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the pubic bone Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pubic bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal foot bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal foot bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated alkaline phosphatase of bone origin Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated alkaline phosphatase of bone origin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sclerosis of hand bone Gene Set

From HPO Gene-Disease Associations

genes associated with the sclerosis of hand bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hand bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patchy variation in bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy variation in bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hump-shaped mound of bone in central and posterior portions of vertebral endplate Gene Set

From HPO Gene-Disease Associations

genes associated with the hump-shaped mound of bone in central and posterior portions of vertebral endplate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bone marrow hypocellularity Gene Set

From HPO Gene-Disease Associations

genes associated with the bone marrow hypocellularity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of limb bone morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of limb bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the zygomatic bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the zygomatic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent metatarsal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the absent metatarsal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of bone marrow cell morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of bone marrow cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bone pain Gene Set

From HPO Gene-Disease Associations

genes associated with the bone pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Giant Cell Tumor of Bone Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Giant Cell Tumor of Bone phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bone Diseases, Metabolic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bone Diseases, Metabolic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bone Diseases, Developmental Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bone Diseases, Developmental phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bone Marrow Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bone Marrow Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bone Marrow Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bone Marrow Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bone Demineralization, Pathologic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bone Demineralization, Pathologic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fractures, Bone Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fractures, Bone phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bone Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bone Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bone Resorption Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bone Resorption phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Neoplasms, Bone Tissue Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neoplasms, Bone Tissue phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fibrous Dysplasia of Bone Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fibrous Dysplasia of Bone phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bone Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bone Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bone Conduction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bone Conduction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Alveolar Bone Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Alveolar Bone Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bone sialoprotein II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bone sialoprotein II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Bone morphogenetic protein 15 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bone morphogenetic protein 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Bone morphogenetic protein 3/3B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bone morphogenetic protein 3/3B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Bone morphogenetic protein 1/tolloid-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bone morphogenetic protein 1/tolloid-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Bone morphogenetic protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bone morphogenetic protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Bone morphogenetic protein receptor type-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bone morphogenetic protein receptor type-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Bone marrow stromal antigen 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bone marrow stromal antigen 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased bone mineral density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased bone mineral density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone mineral density of femur Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone mineral density of femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone marrow cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vomer bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vomer bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short nasal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short nasal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long bone metaphysis morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone healing Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone healing phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small nasal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small nasal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small alisphenoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small alisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased trabecular bone connectivity density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased trabecular bone connectivity density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short frontal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short frontal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intramembranous bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small basioccipital bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small basioccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased bone marrow cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent presphenoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent presphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

scapular bone foramen Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the scapular bone foramen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long bone epiphysis morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

palatine bone horizontal plate hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the palatine bone horizontal plate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short squamosal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short squamosal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased trabecular bone thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased trabecular bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased trabecular bone volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased trabecular bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hyoid bone body morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hyoid bone body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone structure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone structure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal trabecular bone thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal trabecular bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hyoid bone greater horns Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hyoid bone greater horns phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased bone resorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased bone resorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal exoccipital bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal exoccipital bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

temporal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the temporal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long bone diaphysis morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long bone diaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal presphenoid bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal presphenoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sesamoid bone of gastrocnemius morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sesamoid bone of gastrocnemius morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased long bone epiphyseal plate size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased long bone epiphyseal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone mineral density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone mineral density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal nasal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal nasal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased bone mineral content Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased bone mineral content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal palatine bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal palatine bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased trabecular bone mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased trabecular bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent alisphenoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent alisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal trabecular bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal trabecular bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone mineral content Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone mineral content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to bone fracture Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to bone fracture phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short zygomatic bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short zygomatic bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small penile bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small penile bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ectopic cranial bone growth Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ectopic cranial bone growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent zygomatic bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent zygomatic bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged nasal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged nasal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal basioccipital bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal basioccipital bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lacrimal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lacrimal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

failure of bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

frontal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the frontal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent nasal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent nasal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone marrow cavity morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone marrow cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent ethmoidal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent ethmoidal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone resorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone resorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal frontal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal frontal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hyoid bone lesser horns Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hyoid bone lesser horns phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small pterygoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small pterygoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal temporal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal temporal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tarsal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal tarsal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal clitoral bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal clitoral bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal gonial bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal gonial bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long bone epiphyseal plate proliferative zone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long bone epiphyseal plate proliferative zone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal trabecular bone volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal trabecular bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent gonial bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent gonial bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased metatarsal bone number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased metatarsal bone number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent palatine bone horizontal plate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent palatine bone horizontal plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

occipital bone foramen Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the occipital bone foramen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal interparietal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal interparietal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small exoccipital bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small exoccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ectopic bone formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ectopic bone formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal trabecular bone mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal trabecular bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

failure of endochondral bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent carpal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent carpal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fusion of basioccipital and basisphenoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fusion of basioccipital and basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hyoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hyoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ethmoidal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ethmoidal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal penile bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal penile bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

palatine bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the palatine bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

gonial bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the gonial bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent bone marrow cell Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent bone marrow cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased bone strength Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased bone strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased compact bone area Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased compact bone area phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased trabecular bone mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased trabecular bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent basisphenoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

alisphenoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the alisphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small interparietal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small interparietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal zygomatic bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal zygomatic bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal metacarpal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal metacarpal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased trabecular bone volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased trabecular bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ossification involved in bone maturation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ossification involved in bone maturation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

frontal bone foramen Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the frontal bone foramen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

basisphenoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the basisphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pterygoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pterygoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal compact bone mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal compact bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone collagen fibril morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone collagen fibril morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone mineral density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone mineral density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

basisphenoid bone foramen Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the basisphenoid bone foramen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal squamosal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal squamosal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hyoid bone greater horn morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hyoid bone greater horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone resorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone resorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal compact bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal compact bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long bone hypertrophic chondrocyte zone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long bone hypertrophic chondrocyte zone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small basisphenoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal supraoccipital bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal supraoccipital bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pectoral girdle bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pectoral girdle bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal compact bone area Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal compact bone area phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased hyoid bone size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased hyoid bone size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased long bone epiphyseal plate size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased long bone epiphyseal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased compact bone area Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased compact bone area phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

metacarpal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the metacarpal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal limb long bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal limb long bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent squamosal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent squamosal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased trabecular bone connectivity density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased trabecular bone connectivity density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

failure of secondary bone resorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of secondary bone resorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent occipital bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent occipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small frontal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small frontal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone marrow cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone marrow cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal metatarsal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal metatarsal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone mineral content Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone mineral content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature intramembranous bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal compact bone volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal compact bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long bone epiphyseal ossification zone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long bone epiphyseal ossification zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent interparietal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent interparietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hyoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hyoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small temporal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small temporal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal palate bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal palate bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hyoid bone lesser horn morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hyoid bone lesser horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

nasal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the nasal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed endochondral bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased compact bone thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased compact bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased palatine bone horizontal plate size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased palatine bone horizontal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

wide frontal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the wide frontal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone marrow cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent supraoccipital bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent supraoccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased compact bone volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased compact bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased compact bone volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased compact bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pterygoid bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pterygoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged interparietal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged interparietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged frontal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged frontal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vomer bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vomer bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short presphenoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short presphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small supraoccipital bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small supraoccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

broad nasal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the broad nasal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal palatine bone horizontal plate morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal palatine bone horizontal plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal occipital bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal occipital bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal compact bone lamellar structure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal compact bone lamellar structure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal interfrontal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal interfrontal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

scapular bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the scapular bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased compact bone mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased compact bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small occipital bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small occipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone marrow development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone marrow development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone trabecula morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone trabecula morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased bone mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone remodeling Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone remodeling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased metacarpal bone number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased metacarpal bone number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal limb bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal limb bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased trabecular bone thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased trabecular bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

palate bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the palate bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased bone volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sphenoid bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sphenoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent bone trabeculae Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent bone trabeculae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vomer bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vomer bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent palatine bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent palatine bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired ossification of basisphenoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired ossification of basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small zygomatic bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small zygomatic bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal carpal bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal carpal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal orbitosphenoid bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal orbitosphenoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone marrow morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone marrow morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal alisphenoid bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal alisphenoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone strength Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

interparietal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the interparietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long bone epiphyseal plate morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long bone epiphyseal plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thickened long bone epiphysis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thickened long bone epiphysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent frontal bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent frontal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature endochondral bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent clitoral bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent clitoral bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal craniofacial bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal craniofacial bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

presphenoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the presphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone marrow cell morphology/development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone marrow cell morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized long bone epiphyseal plate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized long bone epiphyseal plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hyoid bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hyoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased hyoid bone size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased hyoid bone size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal basisphenoid bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal basisphenoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased compact bone mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased compact bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal endochondral bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone trabecula number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone trabecula number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed intramembranous bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased compact bone thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased compact bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal trabecular bone connectivity density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal trabecular bone connectivity density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pelvic girdle bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pelvic girdle bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased bone trabecula number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased bone trabecula number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone strength Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal compact bone thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal compact bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged gonial bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged gonial bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

failure of intramembranous bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone mineralization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone mineralization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

bone mineral density qtl18, osteoporosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the bone mineral density qtl18, osteoporosis phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density variability 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density variability 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

diastrophic dysplasia, broad bone-platyspondylic variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the diastrophic dysplasia, broad bone-platyspondylic variant phenotype from the curated OMIM Gene-Disease Associations dataset.

{bone marrow failure, telomere-related, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bone marrow failure, telomere-related, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 11] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 11] phenotype from the curated OMIM Gene-Disease Associations dataset.

{bone mineral density qtl 12, osteoporosis} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bone mineral density qtl 12, osteoporosis} phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 13] Gene Set