Name

abnormality of the musculature of the upper arm Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the musculature of the upper arm Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the upper limbs Gene Set

From HPO Gene-Disease Associations

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

abnormality of the upper arm Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the upper arm Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the musculature of the upper limbs Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the musculature of the limbs Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the thorax Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the pelvis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hip-girdle musculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the lower limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the musculature of the lower limbs 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.

abnormality of the shoulder girdle musculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of facial musculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the thigh Gene Set

From HPO Gene-Disease Associations

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

abnormality of the abdominal musculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the neck Gene Set

From HPO Gene-Disease Associations

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

abnormality of the calf musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the calf musculature 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.

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.

abnormality of the upper urinary tract Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the upper limb Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of upper limb metaphysis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of upper lip Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper lip 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.

abnormality of the upper limb Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb epiphysis morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb metaphysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb joint Gene Set

From HPO Gene-Disease Associations

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

abnormality of the upper respiratory tract Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper lip vermillion Gene Set

From HPO Gene-Disease Associations

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

abnormality of the upper urinary tract Gene Set

From HPO Gene-Disease Associations

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

musculature Gene Set

From GeneRIF Biological Term Annotations

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

hypoplasia of the musculature Gene Set

From HPO Gene-Disease Associations

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

aplasia of the abdominal wall musculature Gene Set

From HPO Gene-Disease Associations

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

aplasia of the musculature Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the abdominal wall musculature Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the musculature of the pelvis Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the skeletal musculature Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the musculature of the extremities Gene Set

From HPO Gene-Disease Associations

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

amyotrophy of ankle musculature Gene Set

From HPO Gene-Disease Associations

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

amyotrophy involving the shoulder musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the amyotrophy involving the shoulder musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the shoulder musculature Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the abdominal wall musculature Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the musculature of the thigh Gene Set

From HPO Gene-Disease Associations

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

outer dynein arm Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the outer dynein arm cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

inner dynein arm Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

outer dynein arm Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

Armfield X-Linked Mental Retardation Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Armfield X-Linked Mental Retardation Syndrome from the curated CTD Gene-Disease Associations dataset.

armenia Gene Set

From GeneRIF Biological Term Annotations

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

armadillo Gene Set

From GeneRIF Biological Term Annotations

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

armediated Gene Set

From GeneRIF Biological Term Annotations

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

armigeres Gene Set

From GeneRIF Biological Term Annotations

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

armsreview Gene Set

From GeneRIF Biological Term Annotations

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

armd Gene Set

From GeneRIF Biological Term Annotations

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

armc8alpha Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term armc8alpha in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

armediating Gene Set

From GeneRIF Biological Term Annotations

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

armamentarium Gene Set

From GeneRIF Biological Term Annotations

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

armenian Gene Set

From GeneRIF Biological Term Annotations

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

armadillobetacatenin Gene Set

From GeneRIF Biological Term Annotations

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

arms Gene Set

From GeneRIF Biological Term Annotations

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

armus Gene Set

From GeneRIF Biological Term Annotations

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

armtype Gene Set

From GeneRIF Biological Term Annotations

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

armet Gene Set

From GeneRIF Biological Term Annotations

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

armed Gene Set

From GeneRIF Biological Term Annotations

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

arms2loc387715 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term arms2loc387715 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

arm Gene Set

From GeneRIF Biological Term Annotations

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

armspcr Gene Set

From GeneRIF Biological Term Annotations

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

arms2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term arms2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

armc8beta Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term armc8beta in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

armcx2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term armcx2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

arms2htra1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term arms2htra1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

arms2htra Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term arms2htra in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

army Gene Set

From GeneRIF Biological Term Annotations

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

outer dynein arm assembly Gene Set

From GO Biological Process Annotations

genes participating in the outer dynein arm assembly biological process from the curated GO Biological Process Annotations dataset.

inner dynein arm assembly Gene Set

From GO Biological Process Annotations

genes participating in the inner dynein arm assembly biological process from the curated GO Biological Process Annotations dataset.

outer dynein arm Gene Set

From GO Cellular Component Annotations

proteins localized to the outer dynein arm cellular component from the curated GO Cellular Component Annotations dataset.

armadillo repeat domain binding Gene Set

From GO Molecular Function Annotations

genes performing the armadillo repeat domain binding molecular function from the curated GO Molecular Function Annotations dataset.

mesomelic arm shortening Gene Set

From HPO Gene-Disease Associations

genes associated with the mesomelic arm shortening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent outer dynein arms Gene Set

From HPO Gene-Disease Associations

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

absent/shortened outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent/shortened outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

shortened outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the shortened outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dynein arm defect of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the dynein arm defect of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypopigmented skin patches on arms Gene Set

From HPO Gene-Disease Associations

genes associated with the hypopigmented skin patches on arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent/shortened dynein arms Gene Set

From HPO Gene-Disease Associations

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

bowing of the arm Gene Set

From HPO Gene-Disease Associations

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

absent inner and outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent inner and outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent inner dynein arms Gene Set

From HPO Gene-Disease Associations

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

Armet protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Armet protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Armadillo Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Armadillo protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Armadillo-like helical Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Armadillo-like helical protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Armadillo repeat-containing protein 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Armadillo repeat-containing protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Armadillo repeat protein deleted in velo-cardio-facial syndrome Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Armadillo repeat protein deleted in velo-cardio-facial syndrome protein domain from the InterPro Predicted Protein Domain Annotations dataset.

tRNA-binding arm Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the tRNA-binding arm protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Armadillo repeat-containing domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Armadillo repeat-containing domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ku70/Ku80 C-terminal arm Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ku70/Ku80 C-terminal arm protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Armadillo-type fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Armadillo-type fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ARMC3 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for ARMC3 from the NURSA Protein-Protein Interactions dataset.

ARMC8 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for ARMC8 from the NURSA Protein-Protein Interactions dataset.

ARMC7 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for ARMC7 from the NURSA Protein-Protein Interactions dataset.

mental retardation syndrome, x-linked, armfield type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, armfield type phenotype from the curated OMIM Gene-Disease Associations dataset.

ARMCX5 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMCX5 from the Pathway Commons Protein-Protein Interactions dataset.

ARMCX3 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMCX3 from the Pathway Commons Protein-Protein Interactions dataset.

ARMCX2 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMCX2 from the Pathway Commons Protein-Protein Interactions dataset.

ARMCX1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMCX1 from the Pathway Commons Protein-Protein Interactions dataset.

ARMC9 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMC9 from the Pathway Commons Protein-Protein Interactions dataset.

ARMC6 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMC6 from the Pathway Commons Protein-Protein Interactions dataset.

ARMC10 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMC10 from the Pathway Commons Protein-Protein Interactions dataset.

ARMC8 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMC8 from the Pathway Commons Protein-Protein Interactions dataset.

ARMC7 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMC7 from the Pathway Commons Protein-Protein Interactions dataset.

ARMC5 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMC5 from the Pathway Commons Protein-Protein Interactions dataset.

ARMC2 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMC2 from the Pathway Commons Protein-Protein Interactions dataset.

ARMC1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ARMC1 from the Pathway Commons Protein-Protein Interactions dataset.

ARMS-mediated activation Gene Set

From Reactome Pathways

proteins participating in the ARMS-mediated activation pathway from the Reactome Pathways dataset.

arm Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Primary somatosensory area, upper limb, layer 2/3 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

upper dorsal perifornical nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Primary somatosensory area, upper limb Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

upper dorsal lateral hypothalamic area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in upper dorsal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

upper basal perifornical nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Primary somatosensory area, upper limb, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb, layer 5 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb, layer 4 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb, layer 6a Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Primary somatosensory area, upper limb, layer 6b Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Primary somatosensory area, upper limb, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

upper basal lateral hypothalamic area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in upper basal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

upper (rostral) rhombic lip_8 pcw_M_13058 Gene Set

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

genes with high or low expression in upper (rostral) rhombic lip_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

upper (rostral) rhombic lip_9 pcw_M_12833 Gene Set

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

genes with high or low expression in upper (rostral) rhombic lip_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

upper (rostral) rhombic lip_9 pcw_M_12833 Gene Set

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

genes with high or low expression in upper (rostral) rhombic lip_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

upper (rostral) rhombic lip_8 pcw_M_13058 Gene Set

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

genes with high or low expression in upper (rostral) rhombic lip_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

upper limb region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in upper limb region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

external granular (germinal) layer of upper rhombic lip Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in external granular (germinal) layer of upper rhombic lip relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

upper (rostral) rhombic lip Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in upper (rostral) rhombic lip relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Single upper central incisor Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Single upper central incisor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Single upper central incisor Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Single upper central incisor from the curated CTD Gene-Disease Associations dataset.

upper respiratory tract disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

upper respiratory tract disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

mononeuritis of upper limb and mononeuritis multiplex Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mononeuritis of upper limb and mononeuritis multiplex in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

H3K4me3_fibroblast of upper leg skin_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_fibroblast of upper leg skin_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_fibroblast of upper leg skin_hg19_2 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_fibroblast of upper leg skin_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

CTCF_fibroblast of upper leg skin_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_fibroblast of upper leg skin_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_fibroblast of upper leg skin_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_fibroblast of upper leg skin_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

adenocarcinoma of the upper gastrointestinal tract. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma of the upper gastrointestinal tract. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tumours of the upper aerodigestive tract Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tumours of the upper aerodigestive tract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

upper aerodigestive tract cancer Gene Set

From GAD Gene-Disease Associations

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

neoplasms; recurrence; thromboembolism; thrombophilia; upper extremity deep vein thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms; recurrence; thromboembolism; thrombophilia; upper extremity deep vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

upper aerodigestive tract cancers Gene Set

From GAD Gene-Disease Associations

genes associated with the disease upper aerodigestive tract cancers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

upper Gene Set

From GeneRIF Biological Term Annotations

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

Upper aerodigestive tract cancers Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Upper aerodigestive tract cancers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

upper respiratory tract disease Gene Set

From GWASdb SNP-Disease Associations

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

diaphyseal sclerosis of the upper limbs Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the diaphyseal sclerosis of the upper limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

sclerosis of metaphyses of the upper limbs Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sclerosis of metaphyses of the upper limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

anomaly of the upper limb diaphyses Gene Set

From GWASdb SNP-Phenotype Associations

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

increased upper to lower segment ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the increased upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal upper limb muscle weakness Gene Set

From HPO Gene-Disease Associations

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

u-shaped upper lip vermilion Gene Set

From HPO Gene-Disease Associations

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

upper limb metaphyseal widening Gene Set

From HPO Gene-Disease Associations

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

tented upper lip vermilion Gene Set

From HPO Gene-Disease Associations

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

cleft upper lip Gene Set

From HPO Gene-Disease Associations

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

abnormal upper motor neuron morphology Gene Set

From HPO Gene-Disease Associations

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

upper motor neuron dysfunction Gene Set

From HPO Gene-Disease Associations

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

everted upper lip vermilion Gene Set

From HPO Gene-Disease Associations

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

upper eyelid coloboma Gene Set

From HPO Gene-Disease Associations

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

hyporeflexia of upper limbs Gene Set

From HPO Gene-Disease Associations

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

duplication of bones involving the upper extremities Gene Set

From HPO Gene-Disease Associations

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

short upper lip Gene Set

From HPO Gene-Disease Associations

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

synostosis involving bones of the upper limbs Gene Set

From HPO Gene-Disease Associations

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

upper limb postural tremor Gene Set

From HPO Gene-Disease Associations

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

distal upper limb amyotrophy Gene Set

From HPO Gene-Disease Associations

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

abnormal morphology of bones of the upper limbs Gene Set

From HPO Gene-Disease Associations

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

upper limb amyotrophy Gene Set

From HPO Gene-Disease Associations

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

upper limb phocomelia Gene Set

From HPO Gene-Disease Associations

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

recurrent upper and lower respiratory tract infections Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent upper and lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the upper limbs 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.

weakness due to upper motor neuron dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

upper limb spasticity Gene Set

From HPO Gene-Disease Associations

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

proximal upper limb amyotrophy Gene Set

From HPO Gene-Disease Associations

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

abnormal upper to lower segment ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

episodic upper airway obstruction Gene Set

From HPO Gene-Disease Associations

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

thick upper lip vermilion Gene Set

From HPO Gene-Disease Associations

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

flared upper limb metaphysis Gene Set

From HPO Gene-Disease Associations

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

thin upper lip vermilion Gene Set

From HPO Gene-Disease Associations

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

recurrent upper respiratory tract infections Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent upper respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

upper limb muscle weakness Gene Set

From HPO Gene-Disease Associations

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

upper airway obstruction Gene Set

From HPO Gene-Disease Associations

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

upper limb undergrowth Gene Set

From HPO Gene-Disease Associations

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

proximal muscle weakness in upper limbs Gene Set

From HPO Gene-Disease Associations

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

aplasia involving bones of the upper limbs Gene Set

From HPO Gene-Disease Associations

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

contractures of the joints of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the contractures of the joints of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

upper limb muscle hypoplasia Gene Set

From HPO Gene-Disease Associations

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

upper extremity joint dislocation Gene Set

From HPO Gene-Disease Associations

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

Upper Extremity Deformities, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Upper Extremity Deep Vein Thrombosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Upper Extremity Deep Vein Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

absent upper incisors Gene Set

From MPO Gene-Phenotype Associations

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

abnormal upper lip morphology Gene Set

From MPO Gene-Phenotype Associations

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

upper epidermis Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Hypertelorism with esophageal abnormality and hypospadias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset.

congenital nervous system abnormality Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital nervous system abnormality Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

abnormality of glucagon secretion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

gastrin secretion abnormality Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; dna damage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; neoplasms Gene Set

From GAD Gene-Disease Associations

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

cadasil; chromosome aberrations; chromosome abnormality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

torsion abnormality; vascular malformations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease torsion abnormality; vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; lymphocytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

smooth pursuit eye movement abnormality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormality Gene Set

From GeneRIF Biological Term Annotations

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

abnormality of vitamin metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of movement Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the endometrium Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of thyroid morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype 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 the integument Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of vitamin d metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of myeloid leukocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral subcortex Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of divalent inorganic cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

inflammatory abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the stomach Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of central motor function Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the vasculature Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of glycolipid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of connective tissue Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the aortic valve Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cellular immune system Gene Set

From GWASdb SNP-Phenotype Associations

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

hearing abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of immune serum protein physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of leukocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of oral mucosa Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the urethra Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of brain morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the endocrine system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cerebral artery Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the breast Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the autonomic nervous system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the pharynx Gene Set

From GWASdb SNP-Phenotype Associations

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

eeg abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the femur Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the immune system Gene Set

From GWASdb SNP-Phenotype Associations

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

morphological abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of vitamin a metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the calf Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of potassium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the carotid arteries Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of retinal arteries Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the kidney Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of circle of willis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circle of willis phenotype in GWAS datasets from the GWASdb 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.

abnormality of the pituitary gland Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the myocardium Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the biliary system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cell cycle Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of von willebrand factor Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of finger Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the lower limb Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of long bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of thrombocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of neutrophils Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of neutrophils 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.

abnormality of the iris Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the lower urinary tract Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cardiac ventricle Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of thyroid physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of hair pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

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

mesangial abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of vitamin b metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of circulating fibrinogen Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the adrenal glands Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the intestine Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the respiratory system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of phalanx of finger Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral white matter Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the duodenum Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the skull base Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the astrocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the urinary system physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of basophils Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of nervous system morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

functional abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the face Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the male genitalia Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of facial skeleton Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the posterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the gingiva Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the large intestine Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the lung Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of circulating hormone level Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the placenta Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the ankles Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the femoral neck Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the heart valves Gene Set

From GWASdb SNP-Phenotype Associations

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

morphological abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of aromatic amino acid family metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of prenatal development or birth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of eye movement Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral vasculature Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the ovary Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the prostate Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of amino acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of digit Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of limbs Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the testis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the anterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of dental eruption Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the clavicle Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of homocysteine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the knees Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the coronary arteries Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cardiovascular system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin adnexa Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the pleura Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the hair Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of interleukin secretion Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of blood and blood-forming tissues Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of transition element cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of tryptophan metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the head Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of head or neck Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the mandible Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the vertebral column Gene Set

From GWASdb SNP-Phenotype Associations

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

functional respiratory abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional respiratory abnormality 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.

abnormality of humoral immunity Gene Set

From GWASdb SNP-Phenotype Associations

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

neurodevelopmental abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of taste sensation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of renin-angiotensin system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of pancreas physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the skeletal system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of primary teeth Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the thorax Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the thyroid gland Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the abdomen Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebrum Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebrospinal fluid Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the menstrual cycle Gene Set

From GWASdb SNP-Phenotype Associations

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

behavioral abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the oral cavity Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cholesterol metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of granulocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of monovalent inorganic cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the fundus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of forebrain morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the tongue Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of acid-base homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the vertebrae Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the spinal cord Gene Set

From GWASdb SNP-Phenotype Associations

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

vascular skin abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of iron homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cornea Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of refraction Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of blood volume homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of dna repair Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the nose Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of nitrogen compound homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of central nervous system electrophysiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of nervous system physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of erythrocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of liposaccharide metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the femoral neck or head region Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the urinary system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the vasculature of the eye Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the glomerulus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of unsaturated fatty acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiac morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of circulating protein level Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of copper homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

prenatal maternal abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the humeral diaphysis Gene Set

From GWASdb SNP-Phenotype Associations

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

phenotypic abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of reproductive system physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the uterus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of female internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the curvature of the cornea Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the metaphyses Gene Set

From GWASdb SNP-Phenotype Associations

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

functional abnormality of male internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the common coagulation pathway Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of male internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the hypothalamus-pituitary axis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of fatty-acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the genitourinary system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cytokine secretion Gene Set

From GWASdb SNP-Phenotype Associations

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

growth abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the choroid Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the globe Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of radial diaphysis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of sodium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of muscle morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the ear Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the middle ear ossicles Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cells of the monocyte/macrophage lineage Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lower limb joint Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the uvea Gene Set

From GWASdb SNP-Phenotype Associations

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

biliary tract abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the abdominal organs Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the esophagus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the retina Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the penis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of blood circulation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the radius Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of urine homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the costochondral junction Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral cortex Gene Set

From GWASdb SNP-Phenotype Associations

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

venous abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of extrapyramidal motor function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of extrapyramidal motor function 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 the liver Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of proteoglycan metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of fluid regulation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of metabolism/homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the pylorus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of adipose tissue Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the anterior pituitary Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the nasopharynx Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the intervertebral disk Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the stapes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the gallbladder Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the coagulation cascade Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the teeth Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the left ventricle Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of zinc homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of zinc homeostasis 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.

generalized abnormality of skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the generalized abnormality of skin 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 lipid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of b cells Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the left ventricular outflow tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of carbohydrate metabolism/homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of muscle physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the glial cells Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of dental structure Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the ulna Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the femoral head Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of corneal endothelium Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of lymphocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

muscle abnormality related to mitochondrial dysfunction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of corneal thickness Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the mouth Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the vitamin b12 metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vitamin b12 metabolism 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 magnesium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the small intestine Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the genital system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the aorta Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the female genitalia Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the humerus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cardiovascular system physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

morphological abnormality of the central nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of complement system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cells of the erythroid lineage Gene Set

From GWASdb SNP-Phenotype Associations

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

chorioretinal abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of sulfur amino acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of sulfur amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating cortisol level Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of prothrombin Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the curvature of the vertebral column Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of coagulation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cervical spine Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the skull Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of carboxylic acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the pancreas Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skeletal morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the lens Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of b cell physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of body weight Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of temperature regulation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the systemic arterial tree Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the rib cage Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of glycoprotein metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of vitamin e metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cell physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the eye Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the retinal vasculature Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of ion homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the nervous system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of macrophages Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of calcium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of male external genitalia Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of body height Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of polysaccharide metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the intrinsic pathway Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of eosinophils Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the macula Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of epidermal morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of higher mental function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of higher mental function 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.

abnormality of the ribs Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of nucleobase metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the forearm Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of purine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of serum cytokine level Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of immune system physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of circulating leptin level Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the nephron Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of circulating glucocorticoid level Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the level of lipoprotein cholesterol Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the neck Gene Set

From HPO Gene-Disease Associations

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

abnormality of the falx cerebri Gene Set

From HPO Gene-Disease Associations

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

abnormality of myeloid leukocytes Gene Set

From HPO Gene-Disease Associations

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

abnormality of gastrointestinal vasculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of the extraocular muscles Gene Set

From HPO Gene-Disease Associations

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

abnormality of the choanae Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycolipid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of the nasal cavity Gene Set

From HPO Gene-Disease Associations

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

abnormality of the immune system Gene Set

From HPO Gene-Disease Associations

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

abnormality of reticulocytes Gene Set

From HPO Gene-Disease Associations

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

abnormality of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cochlea Gene Set

From HPO Gene-Disease Associations

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

abnormality of von willebrand factor Gene Set

From HPO Gene-Disease Associations

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

abnormality of cardiac ventricle Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebellar peduncle Gene Set

From HPO Gene-Disease Associations

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

abnormality of the intestine Gene Set

From HPO Gene-Disease Associations

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

abnormality of the gingiva Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lung Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the gastrointestinal tract Gene Set

From HPO Gene-Disease Associations

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

abnormality of the basal ganglia Gene Set

From HPO Gene-Disease Associations

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

abnormality of the vena cava Gene Set

From HPO Gene-Disease Associations

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

abnormality of sharpey fibers Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thorax Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hypothalamus-pituitary axis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the head Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hairline Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cornea Gene Set

From HPO Gene-Disease Associations

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

abnormality of the frontal sinuses Gene Set

From HPO Gene-Disease Associations

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

abnormality of metacarpophalangeal joint Gene Set

From HPO Gene-Disease Associations

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

abnormality of the femoral neck or head region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the intrahepatic bile duct Gene Set

From HPO Gene-Disease Associations

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

abnormality of fluid regulation Gene Set

From HPO Gene-Disease Associations

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

abnormality of the philtrum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the dentate nucleus Gene Set

From HPO Gene-Disease Associations

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

abnormality of the fallopian tube Gene Set

From HPO Gene-Disease Associations

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

abnormality of secondary sexual hair Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pineal gland Gene Set

From HPO Gene-Disease Associations

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

abnormality of the crus of the helix Gene Set

From HPO Gene-Disease Associations

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

abnormality of the acetabulum Gene Set

From HPO Gene-Disease Associations

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

abnormality of vision Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sense of smell Gene Set

From HPO Gene-Disease Associations

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

abnormality of central somatosensory evoked potentials Gene Set

From HPO Gene-Disease Associations

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

abnormality of permanent molar morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of permanent molar morphology 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 muscle physiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the parathyroid physiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the corpus callosum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the achilles tendon Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thumb Gene Set

From HPO Gene-Disease Associations

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

abnormality of the myocardium Gene Set

From HPO Gene-Disease Associations

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

abnormality of complement system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of complement system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease 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.

abnormality of the phalanges of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of glycoprotein metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of blood glucose concentration Gene Set

From HPO Gene-Disease Associations

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

abnormality of the renal tubule Gene Set

From HPO Gene-Disease Associations

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

abnormality of the shoulder Gene Set

From HPO Gene-Disease Associations

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

abnormality of the 3rd toe Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the 3rd toe 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 chromosome condensation Gene Set

From HPO Gene-Disease Associations

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

abnormality of prostaglandin metabolism Gene Set

From HPO Gene-Disease Associations

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

neurodevelopmental abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of connective tissue Gene Set

From HPO Gene-Disease Associations

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

abnormality of thumb phalanx Gene Set

From HPO Gene-Disease Associations

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

abnormality of the odontoid process Gene Set

From HPO Gene-Disease Associations

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

abnormality of alanine metabolism Gene Set

From HPO Gene-Disease Associations

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

atlantoaxial abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lower limb Gene Set

From HPO Gene-Disease Associations

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

abnormality of thrombocytes Gene Set

From HPO Gene-Disease Associations

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

abnormality of the posterior pituitary Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thymus Gene Set

From HPO Gene-Disease Associations

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

abnormality of the anterior chamber Gene Set

From HPO Gene-Disease Associations

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

abnormality of the vestibulocochlear nerve Gene Set

From HPO Gene-Disease Associations

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

abnormality of prenatal development or birth Gene Set

From HPO Gene-Disease Associations

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

abnormality of binocular vision Gene Set

From HPO Gene-Disease Associations

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

abnormality of the nasal septum Gene Set

From HPO Gene-Disease Associations

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

abnormality of cation homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thyroid gland Gene Set

From HPO Gene-Disease Associations

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

abnormality of the bladder Gene Set

From HPO Gene-Disease Associations

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

abnormality of the alveolar ridges Gene Set

From HPO Gene-Disease Associations

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

abnormality of forebrain morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of cerebral artery Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cerebral artery 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.

abnormality of the choroid plexus Gene Set

From HPO Gene-Disease Associations

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

abnormality of circulating protein level Gene Set

From HPO Gene-Disease Associations

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

abnormality of pancreas morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the seventh cranial nerve Gene Set

From HPO Gene-Disease Associations

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

abnormality of the labia minora Gene Set

From HPO Gene-Disease Associations

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

abnormality of the palmar creases Gene Set

From HPO Gene-Disease Associations

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

biliary tract abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of cells of the lymphoid lineage Gene Set

From HPO Gene-Disease Associations

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

abnormality of the aortic arch Gene Set

From HPO Gene-Disease Associations

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

abnormality of the carpal bones Gene Set

From HPO Gene-Disease Associations

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

generalized abnormality of skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of b cells Gene Set

From HPO Gene-Disease Associations

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

abnormality of cardiac morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the glial cells Gene Set

From HPO Gene-Disease Associations

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

abnormality of peripheral nervous system electrophysiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the aryepiglottic fold Gene Set

From HPO Gene-Disease Associations

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

abnormality of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cells of the erythroid lineage Gene Set

From HPO Gene-Disease Associations

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

abnormality of prothrombin Gene Set

From HPO Gene-Disease Associations

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

abnormality of the phalanges of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of b cell physiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the nervous system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the subungual region Gene Set

From HPO Gene-Disease Associations

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

abnormality of thyroid morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the scalp Gene Set

From HPO Gene-Disease Associations

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

inflammatory abnormality of the skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of the frontal hairline Gene Set

From HPO Gene-Disease Associations

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

abnormality of the retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

abnormality of the renal collecting system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pulmonary vasculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pulmonary vasculature 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.

abnormality of the femoral metaphysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of oral mucosa Gene Set

From HPO Gene-Disease Associations

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

abnormality of peripheral nerves Gene Set

From HPO Gene-Disease Associations

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

abnormality of the acoustic reflex Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the middle ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of potassium homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lip Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pituitary gland Gene Set

From HPO Gene-Disease Associations

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

tubulointerstitial abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of the dental pulp Gene Set

From HPO Gene-Disease Associations

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

abnormality of cysteine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of metabolism/homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thenar eminence Gene Set

From HPO Gene-Disease Associations

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

abnormality of ganglioside metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of the middle phalanges of the toes Gene Set

From HPO Gene-Disease Associations

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

abnormality of humoral immunity Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sixth cranial nerve Gene Set

From HPO Gene-Disease Associations

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

abnormality of calvarial morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hip joint Gene Set

From HPO Gene-Disease Associations

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

abnormality of the humeral metaphyses Gene Set

From HPO Gene-Disease Associations

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

abnormality of urine bicarbonate concentration Gene Set

From HPO Gene-Disease Associations

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

abnormality of the genitourinary system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lymphatic vessels Gene Set

From HPO Gene-Disease Associations

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

abnormality of the fascia Gene Set

From HPO Gene-Disease Associations

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

abnormality of the ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of femoral epiphysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the radius Gene Set

From HPO Gene-Disease Associations

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

abnormality of the liver Gene Set

From HPO Gene-Disease Associations

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

abnormality of dental color Gene Set

From HPO Gene-Disease Associations

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

abnormality of alkaline phosphatase activity Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphyses of the distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the distal phalanx of finger 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.

abnormality of the larynx Gene Set

From HPO Gene-Disease Associations

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

chorioretinal abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of circulating hormone level Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the central nervous system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the salivary glands Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cell physiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of primary molar morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of copper homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sacroiliac joint Gene Set

From HPO Gene-Disease Associations

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

abnormality of the diaphragm Gene Set

From HPO Gene-Disease Associations

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

abnormality of movement Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lacrimal duct Gene Set

From HPO Gene-Disease Associations

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

abnormality of the proximal tibial epiphysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the aortic valve Gene Set

From HPO Gene-Disease Associations

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

abnormality of the corticospinal tract Gene Set

From HPO Gene-Disease Associations

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

abnormality of the endocrine system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the tarsal bones Gene Set

From HPO Gene-Disease Associations

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

abnormality of the soft palate Gene Set

From HPO Gene-Disease Associations

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

abnormality of the adrenal glands Gene Set

From HPO Gene-Disease Associations

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

abnormality of the periorbital region Gene Set

From HPO Gene-Disease Associations

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

abnormality of the respiratory system Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of fontanelles Gene Set

From HPO Gene-Disease Associations

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

abnormality of the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

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

abnormality of the septum pellucidum Gene Set

From HPO Gene-Disease Associations

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

abnormality of renal excretion Gene Set

From HPO Gene-Disease Associations

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

abnormality of the premaxilla Gene Set

From HPO Gene-Disease Associations

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

eeg abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of renin-angiotensin system Gene Set

From HPO Gene-Disease Associations

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

abnormality of pancreas physiology Gene Set

From HPO Gene-Disease Associations

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

c1-c2 vertebral abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the c1-c2 vertebral abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of lower lip Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pectoral muscle Gene Set

From HPO Gene-Disease Associations

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

abnormality of descemet's membrane Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sclera Gene Set

From HPO Gene-Disease Associations

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

phenotypic abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of circulating adrenocorticotropin level Gene Set

From HPO Gene-Disease Associations

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

abnormality of the radial head Gene Set

From HPO Gene-Disease Associations

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

abnormality of saccadic eye movements Gene Set

From HPO Gene-Disease Associations

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

abnormality of the nasolabial region Gene Set

From HPO Gene-Disease Associations

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

abnormality of somatosensory evoked potentials Gene Set

From HPO Gene-Disease Associations

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

abnormality of the uvea Gene Set

From HPO Gene-Disease Associations

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

abnormality of female external genitalia Gene Set

From HPO Gene-Disease Associations

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

abnormality of tyrosine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of extrapyramidal motor function Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cardiovascular system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the proximal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the rectum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphysis of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of carbohydrate metabolism/homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the ulna Gene Set

From HPO Gene-Disease Associations

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

abnormality of the supraorbital ridges Gene Set

From HPO Gene-Disease Associations

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

abnormality of the coagulation cascade Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycosaminoglycan metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of the extrinsic pathway Gene Set

From HPO Gene-Disease Associations

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

abnormality of skeletal morphology Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the vestibule of the inner ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of skin adnexa Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skin adnexa 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.

abnormality of the mitral valve Gene Set

From HPO Gene-Disease Associations

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

abnormality of orotic acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of neutrophil physiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of globe location Gene Set

From HPO Gene-Disease Associations

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

abnormality of the scapula Gene Set

From HPO Gene-Disease Associations

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

abnormality of t cells Gene Set

From HPO Gene-Disease Associations

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

abnormality of dicarboxylic acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of cells of the granulocytic lineage Gene Set

From HPO Gene-Disease Associations

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

abnormality of the femur Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pancreatic islet cells Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pancreatic islet cells 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.

abnormality of the lymphatic system Gene Set

From HPO Gene-Disease Associations

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

mesangial abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphyses of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the patella Gene Set

From HPO Gene-Disease Associations

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

blood group antigen abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycolysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the optic disc Gene Set

From HPO Gene-Disease Associations

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

abnormality of dermal melanosomes Gene Set

From HPO Gene-Disease Associations

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

abnormality of leucine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of b cell number Gene Set

From HPO Gene-Disease Associations

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

abnormality of the renal cortex Gene Set

From HPO Gene-Disease Associations

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

abnormality of the ventricular septum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the fetal cardiovascular system Gene Set

From HPO Gene-Disease Associations

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

abnormality of nitrogen compound homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the 3rd metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the palate Gene Set

From HPO Gene-Disease Associations

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

abnormality of the posterior hairline Gene Set

From HPO Gene-Disease Associations

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

abnormality of the mandible Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sinuses Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pubic hair Gene Set

From HPO Gene-Disease Associations

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

abnormality of proteoglycan metabolism Gene Set

From HPO Gene-Disease Associations

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

muscle abnormality related to mitochondrial dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the macula Gene Set

From HPO Gene-Disease Associations

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

abnormality of the styloid process of ulna Gene Set

From HPO Gene-Disease Associations

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

abnormality of skull ossification Gene Set

From HPO Gene-Disease Associations

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

abnormality of vision evoked potentials Gene Set

From HPO Gene-Disease Associations

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

abnormality of the labia majora Gene Set

From HPO Gene-Disease Associations

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

abnormality of the genital system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the humerus Gene Set

From HPO Gene-Disease Associations

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

abnormality of lens shape Gene Set

From HPO Gene-Disease Associations

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

abnormality of the eye Gene Set

From HPO Gene-Disease Associations

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

abnormality of the uvula Gene Set

From HPO Gene-Disease Associations

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

abnormality of lateral ventricle Gene Set

From HPO Gene-Disease Associations

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

abnormality of chromosome segregation Gene Set

From HPO Gene-Disease Associations

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

abnormality of higher mental function Gene Set

From HPO Gene-Disease Associations

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

inflammatory abnormality of the eye Gene Set

From HPO Gene-Disease Associations

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

abnormality of vitamin k metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of vitamin k metabolism 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.

abnormality of the conjunctiva Gene Set

From HPO Gene-Disease Associations

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

abnormality of amino acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of the chin Gene Set

From HPO Gene-Disease Associations

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

abnormality of cardiac atrium Gene Set

From HPO Gene-Disease Associations

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

abnormality of pain sensation Gene Set

From HPO Gene-Disease Associations

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

abnormality of the distal femoral epiphysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the menstrual cycle Gene Set

From HPO Gene-Disease Associations

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

abnormality of the anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior fontanelle 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 pyruvate family amino acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of pyruvate family amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sacrococcygeal pilonidal abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of adrenal morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of adrenal morphology 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.

abnormality of male internal genitalia Gene Set

From HPO Gene-Disease Associations

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

abnormality of the eyelashes Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral vasculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of urine hormone level Gene Set

From HPO Gene-Disease Associations

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

abnormality of mast cells Gene Set

From HPO Gene-Disease Associations

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

abnormality of globe size Gene Set

From HPO Gene-Disease Associations

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

abnormality of the eyebrow Gene Set

From HPO Gene-Disease Associations

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

vascular skin abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of central nervous system electrophysiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the foramen magnum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the phalanges of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the inner ear 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.

abnormality of the urinary system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the dorsal column of the spinal cord Gene Set

From HPO Gene-Disease Associations

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