Name

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.

split-hand/foot malformation with long bone deficiency 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 3 phenotype from the curated OMIM 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.

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.

split-hand/foot malformation with long bone deficiency 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation with long bone deficiency 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

Split-hand/foot malformation 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-Hand/Foot Malformation 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation 6 from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation 4 from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation 5 from the curated CTD Gene-Disease Associations dataset.

SPLIT-HAND/FOOT MALFORMATION 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPLIT-HAND/FOOT MALFORMATION 2 from the curated CTD Gene-Disease Associations dataset.

split hand/foot malformation 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split hand/foot malformation 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

split hand/foot malformation 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split hand/foot malformation 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

?split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 3, gene duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 3, gene duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

Split hand foot deformity 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split hand foot deformity 1 from the curated CTD Gene-Disease Associations dataset.

split foot Gene Set

From HPO Gene-Disease Associations

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

Capillary malformation without arteriovenous malformation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Capillary malformation without arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Capillary malformation-arteriovenous malformation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Capillary malformation-arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Capillary Malformation-Arteriovenous Malformation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Capillary Malformation-Arteriovenous Malformation from the curated CTD Gene-Disease Associations dataset.

capillary malformation-arteriovenous malformation Gene Set

From OMIM Gene-Disease Associations

genes associated with the capillary malformation-arteriovenous malformation phenotype from the curated OMIM Gene-Disease Associations dataset.

split hand Gene Set

From HPO Gene-Disease Associations

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

Hand foot uterus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hand foot uterus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hand foot uterus syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hand foot uterus syndrome from the curated CTD Gene-Disease Associations dataset.

hand, foot and mouth disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease hand, foot and mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

hand, foot and mouth disease Gene Set

From GWASdb SNP-Disease Associations

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

Hand, Foot and Mouth Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hand, Foot and Mouth Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

hand-foot-uterus syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the hand-foot-uterus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

long foot Gene Set

From HPO Gene-Disease Associations

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

deviation of the hand or of fingers of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

radial deviation of the hand or of fingers of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the radial deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ulnar deviation of the hand or of fingers of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the ulnar deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease 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.

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.

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.

long-chain-(s)-2-hydroxy-long-chain-acid oxidase activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain-(s)-2-hydroxy-long-chain-acid oxidase activity molecular function from the curated GO Molecular Function Annotations 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.

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 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.

factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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.

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.

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.

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 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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

long bone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Very long chain acyl-CoA dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Very long chain acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

long chain 3 hydroxyacyl coa dehydrogenase deficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the long chain 3 hydroxyacyl coa dehydrogenase deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

split Gene Set

From GeneRIF Biological Term Annotations

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

Sensory disturbances after bilateral sagittal split ramus osteotomy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Sensory disturbances after bilateral sagittal split ramus osteotomy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

junctional split Gene Set

From HPO Gene-Disease Associations

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

split nail Gene Set

From HPO Gene-Disease Associations

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

TUP1-like enhancer of split Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TUP1-like enhancer of split protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FMN-binding split barrel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FMN-binding split barrel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

split cervical atlas Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the split cervical atlas phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

split notochord Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the split notochord phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

split sternal manubrium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the split sternal manubrium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

split vertebrae Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the split vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

split cervical axis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the split cervical axis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

split sternum Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the split sternum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

split xiphoid process Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the split xiphoid process 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.

Dandy-Walker like malformation with atrioventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Malformation of the heart Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Malformation of the heart phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly-capillary malformation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly-capillary malformation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arnold-Chiari Malformation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arnold-Chiari Malformation from the curated CTD Gene-Disease Associations dataset.

arteriovenous malformation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

arteriovenous malformations; congenital arteriovenous malformation; intracranial hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriovenous malformations; congenital arteriovenous malformation; intracranial hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chiari type i malformation and syringomyelia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chiari type i malformation and syringomyelia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriovenous malformations; congenital arteriovenous malformation; hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriovenous malformations; congenital arteriovenous malformation; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intracranial arteriovenous malformation; intracranial arteriovenous malformations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intracranial arteriovenous malformation; intracranial arteriovenous malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

wilms' tumor and congenital male genitourinary malformation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease wilms' tumor and congenital male genitourinary malformation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; intracranial arteriovenous malformation; intracranial arteriovenous malformations; intracranial hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammation; intracranial arteriovenous malformation; intracranial arteriovenous malformations; intracranial hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic nerve malformation Gene Set

From GAD Gene-Disease Associations

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

malformation Gene Set

From GeneRIF Biological Term Annotations

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

Congenital heart malformation Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

thyroid malformation Gene Set

From GWASdb SNP-Disease Associations

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

malformation of the heart and great vessels Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the malformation of the heart and great vessels phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

malformation of the heart and great vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the malformation of the heart and great vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

external ear malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the external ear malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gastrointestinal arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the gastrointestinal arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the hepatic arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebral arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

arnold-chiari malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the arnold-chiari malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital malformation of the great arteries Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital malformation of the great arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cochlear malformation Gene Set

From HPO Gene-Disease Associations

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

retinal vascular malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal vascular malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

arnold-chiari type i malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the arnold-chiari type i malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulmonary arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

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

retinal malformation Gene Set

From HPO Gene-Disease Associations

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

malformation of the hepatic ductal plate Gene Set

From HPO Gene-Disease Associations

genes associated with the malformation of the hepatic ductal plate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

venous malformation Gene Set

From HPO Gene-Disease Associations

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

dandy-walker malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the dandy-walker malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital malformation of the right heart Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital malformation of the right heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital malformation of the left heart Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital malformation of the left heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

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

cerebellar malformation Gene Set

From HPO Gene-Disease Associations

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

Arnold-Chiari Malformation Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Arnold-Chiari Malformation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

cerebral arteriovenous malformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cerebral arteriovenous malformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pulmonary arteriovenous malformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pulmonary arteriovenous malformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

arteriovenous malformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the arteriovenous malformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

microcephaly-capillary malformation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly-capillary malformation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

megalencephaly-capillary malformation-polymicrogyria syndrome, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the megalencephaly-capillary malformation-polymicrogyria syndrome, somatic phenotype from the curated OMIM 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.

glial limiting end-foot Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the glial limiting end-foot cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

astrocyte end-foot Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the astrocyte end-foot cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

astrocyte end-foot Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the astrocyte end-foot cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

foot layer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the foot layer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Foot Dermatoses Gene Set

From CTD Gene-Disease Associations

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

Foot Deformities, Congenital Gene Set

From CTD Gene-Disease Associations

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

diabetic foot Gene Set

From GAD Gene-Disease Associations

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

diabetes complications; diabetic angiopathies; diabetic foot; syndrome; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; diabetic angiopathies; diabetic foot; syndrome; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; diabetic foot; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; diabetic foot; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

foot Gene Set

From GeneRIF Biological Term Annotations

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

glial limiting end-foot Gene Set

From GO Cellular Component Annotations

proteins localized to the glial limiting end-foot cellular component from the curated GO Cellular Component Annotations dataset.

astrocyte end-foot Gene Set

From GO Cellular Component Annotations

proteins localized to the astrocyte end-foot cellular component from the curated GO Cellular Component Annotations dataset.

foot dorsiflexor weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the foot dorsiflexor weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

foot polydactyly Gene Set

From HPO Gene-Disease Associations

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

narrow foot Gene Set

From HPO Gene-Disease Associations

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

abnormality of the plantar skin of foot Gene Set

From HPO Gene-Disease Associations

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

abnormality of the foot Gene Set

From HPO Gene-Disease Associations

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

positional foot deformity Gene Set

From HPO Gene-Disease Associations

genes associated with the positional foot deformity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

preaxial foot polydactyly Gene Set

From HPO Gene-Disease Associations

genes associated with the preaxial foot polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

rocker bottom foot Gene Set

From HPO Gene-Disease Associations

genes associated with the rocker bottom foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital foot contractures Gene Set

From HPO Gene-Disease Associations

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

abnormality of the foot musculature Gene Set

From HPO Gene-Disease Associations

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

short foot Gene Set

From HPO Gene-Disease Associations

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

broad foot Gene Set

From HPO Gene-Disease Associations

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

medial deviation of the foot Gene Set

From HPO Gene-Disease Associations

genes associated with the medial deviation of the foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

valgus foot deformity Gene Set

From HPO Gene-Disease Associations

genes associated with the valgus foot deformity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

postaxial polysyndactyly of foot Gene Set

From HPO Gene-Disease Associations

genes associated with the postaxial polysyndactyly of foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

postaxial foot polydactyly Gene Set

From HPO Gene-Disease Associations

genes associated with the postaxial foot polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mesoaxial foot polydactyly Gene Set

From HPO Gene-Disease Associations

genes associated with the mesoaxial foot polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Foot Dermatoses Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Foot Dermatoses phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Foot Ulcer Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Foot Ulcer phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Diabetic Foot Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Diabetic Foot phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Foot Deformities, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abnormal hind foot hair pigmentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hind foot hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal foot pigmentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal foot pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fused podocyte foot processes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fused podocyte foot processes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent podocyte foot process Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent podocyte foot process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

podocyte foot process effacement Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the podocyte foot process effacement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dark foot pads Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dark foot pads phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal foot pad morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal podocyte foot process morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal podocyte foot process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal foot plate morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased foot pigmentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased foot pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

charcot-marie-tooth disease, foot deformity of Gene Set

From OMIM Gene-Disease Associations

genes associated with the charcot-marie-tooth disease, foot deformity of phenotype from the curated OMIM Gene-Disease Associations dataset.

synpolydactyly with foot anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the synpolydactyly with foot anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

foot Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue foot from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

foot sole Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue foot sole from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

foot muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

foot sole Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

foot Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

tube foot Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Neuraminidase deficiency with beta-galactosidase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choline deficiency; dna damage; folic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

protein c deficiency; protein s deficiency; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.

Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.

Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.

Spondylometaepiphyseal dysplasia short limb-hand type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaepiphyseal dysplasia short limb-hand type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heart-hand syndrome, Slovenian type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart-hand syndrome, Slovenian type from the curated CTD Gene-Disease Associations dataset.

Craniofacial deafness hand syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniofacial deafness hand syndrome from the curated CTD Gene-Disease Associations dataset.

Hand Dermatoses Gene Set

From CTD Gene-Disease Associations

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

Hand Deformities, Congenital Gene Set

From CTD Gene-Disease Associations

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

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type from the curated CTD Gene-Disease Associations dataset.

Hand Strength Gene Set

From dbGAP Gene-Trait Associations

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

hand dermatosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dermatitis, contact; hand dermatoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatitis, contact; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dermatitis, atopic; eczema; eczema allergic; hand dermatoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatitis, atopic; eczema; eczema allergic; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hand strength Gene Set

From GAD Gene-Disease Associations

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

dermatitis, allergic contact; hand dermatoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatitis, allergic contact; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart-hand syndrome, holt-oram syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dermatitis, atopic; dermatitis, irritant; dermatitis, occupational; hand dermatoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatitis, atopic; dermatitis, irritant; dermatitis, occupational; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hand Gene Set

From GeneRIF Biological Term Annotations

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

Relative hand skill in reading disability Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Relative hand skill in reading disability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormality of the hand Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal ossification of hand bones Gene Set

From HPO Gene-Disease Associations

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

irregular sclerosis of hand bones Gene Set

From HPO Gene-Disease Associations

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

bracket epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

enlarged epiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

aplasia of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the proximal 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 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.

hypotrophy of the small hand muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the hypotrophy of the small hand muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patchy sclerosis of hand bones Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

aplasia of the middle phalanx of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the middle phalanx of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

partial duplication of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

hand tremor Gene Set

From HPO Gene-Disease Associations

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

duplication of the distal phalanx of hand Gene Set

From HPO Gene-Disease Associations

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

enlarged epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

broad phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

valgus hand deformity Gene Set

From HPO Gene-Disease Associations

genes associated with the valgus hand deformity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

radial deviation of the hand Gene Set

From HPO Gene-Disease Associations

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

hand clenching Gene Set

From HPO Gene-Disease Associations

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

triangular epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

cold-induced hand cramps Gene Set

From HPO Gene-Disease Associations

genes associated with the cold-induced hand cramps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

triangular shaped proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

hand muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of hand joint mobility Gene Set

From HPO Gene-Disease Associations

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

triangular epiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hand Gene Set

From HPO Gene-Disease Associations

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

bullet-shaped phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

triangular shaped distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

complete duplication of phalanx of hand Gene Set

From HPO Gene-Disease Associations

genes associated with the complete duplication of phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent hand Gene Set

From HPO Gene-Disease Associations

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

ulnar deviation of the hand Gene Set

From HPO Gene-Disease Associations

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

irregular ossification of hand bones Gene Set

From HPO Gene-Disease Associations

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

thimble-shaped middle phalanges of hand Gene Set

From HPO Gene-Disease Associations

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

duplication of hand bones Gene Set

From HPO Gene-Disease Associations

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

duplication of phalanx of hand Gene Set

From HPO Gene-Disease Associations

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

symphalangism affecting the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

ivory epiphyses of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

pseudoepiphyses of hand bones Gene Set

From HPO Gene-Disease Associations

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

bracket epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

weakness of the intrinsic hand muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the weakness of the intrinsic hand muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hyperextensible hand joints Gene Set

From HPO Gene-Disease Associations

genes associated with the hyperextensible hand joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular epiphyses of the middle phalanges of the hand 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.

aplasia/hypoplasia of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

joint contracture of the hand Gene Set

From HPO Gene-Disease Associations

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

complete duplication of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

cone-shaped epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

synostosis involving bones of the hand Gene Set

From HPO Gene-Disease Associations

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

mesoaxial hand polydactyly Gene Set

From HPO Gene-Disease Associations

genes associated with the mesoaxial hand polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

symphalangism affecting the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormal hand morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hand morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

complete duplication of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

poor hand-eye coordination Gene Set

From HPO Gene-Disease Associations

genes associated with the poor hand-eye coordination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

duplication of the middle phalanx of hand Gene Set

From HPO Gene-Disease Associations

genes associated with the duplication of the middle phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

small hand Gene Set

From HPO Gene-Disease Associations

genes associated with the small hand 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.

enlarged epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

cone-shaped epiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

trident hand Gene Set

From HPO Gene-Disease Associations

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

thin proximal phalanges with broad epiphyses of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the thin proximal phalanges with broad epiphyses of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hand polydactyly Gene Set

From HPO Gene-Disease Associations

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

cone-shaped epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the cone-shaped epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

preaxial hand polydactyly Gene Set

From HPO Gene-Disease Associations

genes associated with the preaxial hand polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bullet-shaped middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of phalangeal joints of the hand Gene Set

From HPO Gene-Disease Associations

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

aplasia of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

partial duplication of the phalanx of hand Gene Set

From HPO Gene-Disease Associations

genes associated with the partial duplication of the phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphyses of the hand Gene Set

From HPO Gene-Disease Associations

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

radial club hand Gene Set

From HPO Gene-Disease Associations

genes associated with the radial club hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short tubular bones (hand) Gene Set

From HPO Gene-Disease Associations

genes associated with the short tubular bones (hand) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pseudoepiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

ivory epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

postaxial hand polydactyly Gene Set

From HPO Gene-Disease Associations

genes associated with the postaxial hand polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pseudoepiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the hand Gene Set

From HPO Gene-Disease Associations

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

hand muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the hand muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hand Deformities, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

IQ motif, EF-hand binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the IQ motif, EF-hand binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand, Ca insensitive Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand, Ca insensitive protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ISWI, HAND domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ISWI, HAND domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF hand associated, type-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF hand associated, type-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF hand associated, type-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF hand associated, type-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand domain pair Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand domain pair protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-Hand 1, calcium-binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-Hand 1, calcium-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phospholipase C, phosphoinositol-specific, EF-hand-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phospholipase C, phosphoinositol-specific, EF-hand-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Adaptor protein Cbl, EF hand-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adaptor protein Cbl, EF hand-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand calcium-binding domain-containing protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand calcium-binding domain-containing protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand domain, type 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand domain, type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand domain, type 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand domain, type 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

spondylometaepiphyseal dysplasia, short limb-hand type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaepiphyseal dysplasia, short limb-hand type phenotype from the curated OMIM Gene-Disease Associations dataset.

heart-hand syndrome, slovenian type Gene Set

From OMIM Gene-Disease Associations

genes associated with the heart-hand syndrome, slovenian type phenotype from the curated OMIM Gene-Disease Associations dataset.

craniofacial-deafness-hand syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial-deafness-hand syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

hand Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

long insular gyri, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in long insular gyri, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

long insular gyri, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in long insular gyri, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

the prc2 complex sets long-term gene silencing through modification of histone tails Gene Set

From Biocarta Pathways

proteins participating in the the prc2 complex sets long-term gene silencing through modification of histone tails pathway from the Biocarta Pathways dataset.

Long QT syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Long QT syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Long QT syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Long QT syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Long QT syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Long QT syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Long QT syndrome 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Long QT syndrome 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Long QT syndrome 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Long QT syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Long QT syndrome 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Long QT syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acquired long QT syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acquired long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LONG QT SYNDROME 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the LONG QT SYNDROME 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital long QT syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Long QT syndrome 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Long QT syndrome 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Long Qt Syndrome 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long Qt Syndrome 9 from the curated CTD Gene-Disease Associations dataset.

Long QT Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long QT Syndrome from the curated CTD Gene-Disease Associations dataset.

Long QT syndrome type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long QT syndrome type 3 from the curated CTD Gene-Disease Associations dataset.

Long Qt Syndrome 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long Qt Syndrome 5 from the curated CTD Gene-Disease Associations dataset.

Long Qt Syndrome 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long Qt Syndrome 6 from the curated CTD Gene-Disease Associations dataset.

Long Qt Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long Qt Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Long Qt Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long Qt Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Long Qt Syndrome 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long Qt Syndrome 10 from the curated CTD Gene-Disease Associations dataset.

Long Qt Syndrome 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long Qt Syndrome 11 from the curated CTD Gene-Disease Associations dataset.

Long Qt Syndrome 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long Qt Syndrome 12 from the curated CTD Gene-Disease Associations dataset.

LONG QT SYNDROME 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LONG QT SYNDROME 13 from the curated CTD Gene-Disease Associations dataset.

Triglyceride storage disease with impaired long-chain fatty acid oxidation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Triglyceride storage disease with impaired long-chain fatty acid oxidation from the curated CTD Gene-Disease Associations dataset.

long qt syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

long qt syndrome Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

long qt syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

human long-term memory Gene Set

From GAD Gene-Disease Associations

genes associated with the disease human long-term memory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inherited cardiac arrhythmia long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inherited cardiac arrhythmia long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; diabetic angiopathies; long qt syndrome; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; diabetic angiopathies; long qt syndrome; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced long-qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced long-qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

long qt syndrome; torsades de pointes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease long qt syndrome; torsades de pointes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

long-qt syndrome Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; heart arrest; long qt syndrome; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; heart arrest; long qt syndrome; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disease models, animal; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disease models, animal; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

long qt syndrome; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease long qt syndrome; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

long qt syndrome Gene Set

From GAD Gene-Disease Associations

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

delayed graft function acute rejection episodes and long-term graft dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease delayed graft function acute rejection episodes and long-term graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; death, sudden; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

long qt syndrome; sinus tachycardia; tachycardia, sinus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease long qt syndrome; sinus tachycardia; tachycardia, sinus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

depression ; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depression ; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

long-term kidney allograft survival Gene Set

From GAD Gene-Disease Associations

genes associated with the disease long-term kidney allograft survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

long Gene Set

From GeneRIF Biological Term Annotations

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

long-chain fatty acid catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations dataset.

long-chain fatty-acyl-coa biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the long-chain fatty-acyl-coa biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

very long-chain fatty-acyl-coa metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the very long-chain fatty-acyl-coa metabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of long term synaptic depression Gene Set

From GO Biological Process Annotations

genes participating in the regulation of long term synaptic depression biological process from the curated GO Biological Process Annotations dataset.

plasma membrane long-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

regulation of long-term synaptic potentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations dataset.

long-chain fatty acid import Gene Set

From GO Biological Process Annotations

genes participating in the long-chain fatty acid import biological process from the curated GO Biological Process Annotations dataset.

very long-chain fatty acid metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the very long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations dataset.

long-chain fatty-acyl-coa metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the long-chain fatty-acyl-coa metabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of plasma membrane long-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

long-term memory Gene Set

From GO Biological Process Annotations

genes participating in the long-term memory biological process from the curated GO Biological Process Annotations dataset.

long-chain fatty-acyl-coa catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the long-chain fatty-acyl-coa catabolic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of long-term synaptic potentiation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations dataset.

regulation of long-term neuronal synaptic plasticity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations dataset.

long term synaptic depression Gene Set

From GO Biological Process Annotations

genes participating in the long term synaptic depression biological process from the curated GO Biological Process Annotations dataset.

long-chain fatty acid biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

long-term synaptic potentiation Gene Set

From GO Biological Process Annotations

genes participating in the long-term synaptic potentiation biological process from the curated GO Biological Process Annotations dataset.

long-chain fatty acid metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the long-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations dataset.

negative regulation of long term synaptic depression Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of long term synaptic depression biological process from the curated GO Biological Process Annotations dataset.

long-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the long-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

positive regulation of long-term neuronal synaptic plasticity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations dataset.

peroxisomal long-chain fatty acid import Gene Set

From GO Biological Process Annotations

genes participating in the peroxisomal long-chain fatty acid import biological process from the curated GO Biological Process Annotations dataset.

positive regulation of plasma membrane long-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of plasma membrane long-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of plasma membrane long-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

very long-chain fatty acid biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the very long-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

very long-chain fatty acid catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the very long-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations dataset.

long-chain-enoyl-coa hydratase activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain-enoyl-coa hydratase activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain acyl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain acyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain fatty acid-coa ligase activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain fatty acid-coa ligase activity molecular function from the curated GO Molecular Function Annotations dataset.

very-long-chain-(s)-2-hydroxy-acid oxidase activity Gene Set

From GO Molecular Function Annotations

genes performing the very-long-chain-(s)-2-hydroxy-acid oxidase activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain fatty acid binding Gene Set

From GO Molecular Function Annotations

genes performing the long-chain fatty acid binding molecular function from the curated GO Molecular Function Annotations dataset.

long-chain-alcohol oxidase activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain-alcohol o-fatty-acyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain-alcohol o-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain-fatty-acyl-coa reductase activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain-fatty-acyl-coa reductase activity molecular function from the curated GO Molecular Function Annotations dataset.

very long chain acyl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the very long chain acyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

very-long-chain-acyl-coa dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the very-long-chain-acyl-coa dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain-3-hydroxyacyl-coa dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain-3-hydroxyacyl-coa dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain fatty acyl-coa binding Gene Set

From GO Molecular Function Annotations

genes performing the long-chain fatty acyl-coa binding molecular function from the curated GO Molecular Function Annotations dataset.

very long-chain fatty acid-coa ligase activity Gene Set

From GO Molecular Function Annotations

genes performing the very long-chain fatty acid-coa ligase activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain-acyl-coa dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain-acyl-coa dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain fatty acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain fatty acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

long qt syndrome Gene Set

From GWASdb SNP-Disease Associations

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

increased density of long bones Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the increased density of long bones phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the medullary cavity of the long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thickened cortex of long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the thickened cortex of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long face Gene Set

From HPO Gene-Disease Associations

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

fractures of the long bones Gene Set

From HPO Gene-Disease Associations

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

cortically dense long tubular bones Gene Set

From HPO Gene-Disease Associations

genes associated with the cortically dense long tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long neck Gene Set

From HPO Gene-Disease Associations

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

long metacarpals Gene Set

From HPO Gene-Disease Associations

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

long fingers Gene Set

From HPO Gene-Disease Associations

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

long coccyx Gene Set

From HPO Gene-Disease Associations

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

periosteal thickening of long tubular bones Gene Set

From HPO Gene-Disease Associations

genes associated with the periosteal thickening of long tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long fibula Gene Set

From HPO Gene-Disease Associations

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

long proximal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the long proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long penis Gene Set

From HPO Gene-Disease Associations

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

long palm Gene Set

From HPO Gene-Disease Associations

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

long hallux Gene Set

From HPO Gene-Disease Associations

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

increased density of long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the increased density of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

crumpled long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the crumpled long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long second metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the long second metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the long phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

broad long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the broad long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

very long chain fatty acid accumulation Gene Set

From HPO Gene-Disease Associations

genes associated with the very long chain fatty acid accumulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

stenosis of the medullary cavity of the long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the stenosis of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long clavicles Gene Set

From HPO Gene-Disease Associations

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

weakness of long finger extensor muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the weakness of long finger extensor muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bowing of the long bones Gene Set

From HPO Gene-Disease Associations

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

long upper lip Gene Set

From HPO Gene-Disease Associations

genes associated with the long upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long-segment aganglionic megacolon Gene Set

From HPO Gene-Disease Associations

genes associated with the long-segment aganglionic megacolon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated long chain fatty acids Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated long chain fatty acids phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long nose Gene Set

From HPO Gene-Disease Associations

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

long toe Gene Set

From HPO Gene-Disease Associations

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

long thorax Gene Set

From HPO Gene-Disease Associations

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

long-tract signs Gene Set

From HPO Gene-Disease Associations

genes associated with the long-tract signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long palpebral fissure Gene Set

From HPO Gene-Disease Associations

genes associated with the long palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior bowing of long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior bowing of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of long-chain fatty-acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of long-chain fatty-acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

overtubulated long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the overtubulated long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the long distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long ear Gene Set

From HPO Gene-Disease Associations

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

protuberances at ends of long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the protuberances at ends of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long philtrum Gene Set

From HPO Gene-Disease Associations

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

long-chain dicarboxylic aciduria Gene Set

From HPO Gene-Disease Associations

genes associated with the long-chain dicarboxylic aciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long eyelashes in irregular rows Gene Set

From HPO Gene-Disease Associations

genes associated with the long eyelashes in irregular rows phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long eyelashes Gene Set

From HPO Gene-Disease Associations

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

long eyebrows Gene Set

From HPO Gene-Disease Associations

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

Memory, Long-Term Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Memory, Long-Term phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Long QT Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Long QT Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Long hematopoietin receptor, single chain, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Long hematopoietin receptor, single chain, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Long hematopoietin receptor, Gp130 family 2, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Long hematopoietin receptor, Gp130 family 2, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Long hematopoietin receptor, soluble alpha chain, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Long hematopoietin receptor, soluble alpha chain, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

PLUNC, long form Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PLUNC, long form protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peroxysomal long chain fatty acyl transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peroxysomal long chain fatty acyl transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Acyl-CoA thioesterase, long chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Acyl-CoA thioesterase, long chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Anaphase-promoting complex subunit 4 long domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Anaphase-promoting complex subunit 4 long domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

long term depression Gene Set

From KEGG Pathways

proteins participating in the long term depression pathway from the KEGG Pathways dataset.

long term potentiation Gene Set

From KEGG Pathways

proteins participating in the long term potentiation pathway from the KEGG Pathways dataset.

long hair Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent long term depression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enhanced long term potentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enhanced long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long nails Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long nails phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased length of long bones Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased length of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

reduced long term potentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the reduced long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long snout Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long snout phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased diameter of long bones Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased diameter of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long fibula Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long fibula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased length of long bones Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased length of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long gestation period Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long gestation period phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long term object recognition memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long term object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased diameter of long bones Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased diameter of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long radius Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long radius phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long ribs Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long ribs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long lived plasma cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

long tibia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long tibia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long term potentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long mandible Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long mandible phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

reduced long term depression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the reduced long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long tail Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long tail phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long femur Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long stride length Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long stride length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long term spatial reference memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long term spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long ulna Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long ulna phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long humerus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long humerus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long limbs Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long limbs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long term depression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long incisors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long toenails Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the long toenails phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

long qt syndrome 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

long qt syndrome 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

{long qt syndrome 1, acquired, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {long qt syndrome 1, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

long qt syndrome-11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome-11 phenotype from the curated OMIM Gene-Disease Associations dataset.

long qt syndrome-10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome-10 phenotype from the curated OMIM Gene-Disease Associations dataset.

long qt syndrome 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

long qt syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

long qt syndrome 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

long qt syndrome 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

long qt syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

long qt syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

{long qt syndrome 2, acquired, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {long qt syndrome 2, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{long qt syndrome, acquired, reduced susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {long qt syndrome, acquired, reduced susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

long qt syndrome-3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the long qt syndrome-3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Beta-oxidation of very long chain fatty acids Gene Set

From Reactome Pathways

proteins participating in the Beta-oxidation of very long chain fatty acids pathway from the Reactome Pathways dataset.

Repair synthesis of patch ~27-30 bases long by DNA polymerase Gene Set

From Reactome Pathways

proteins participating in the Repair synthesis of patch ~27-30 bases long by DNA polymerase pathway from the Reactome Pathways dataset.

Synthesis of very long-chain fatty acyl-CoAs Gene Set

From Reactome Pathways

proteins participating in the Synthesis of very long-chain fatty acyl-CoAs pathway from the Reactome Pathways dataset.

immunodeficiency 32b, monocyte and dendritic cell deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 32b, monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

TG(20:3n6/20:3n6/20:3n6) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the TG(20:3n6/20:3n6/20:3n6) metabolite from the curated HMDB Metabolites of Enzymes 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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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 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