| Name |
|---|
functional abnormality of male internal genitalia Gene SetFrom 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. |
functional abnormality of male internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the functional abnormality of male internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Functional Abnormality Of Male Internal Genitalia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Abnormality Of Male Internal Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
abnormality of male internal genitalia Gene SetFrom 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 male internal genitalia Gene SetFrom 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 Male Internal Genitalia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Male Internal Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
abnormal internal male genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal internal male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent internal male genitalia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent internal male genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent internal male genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent internal male genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal internal male genitalia morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal internal male genitalia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormality of female internal genitalia Gene SetFrom 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 female internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of female internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of Female Internal Genitalia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Female Internal Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
abnormality of the male genitalia Gene SetFrom 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 male external genitalia Gene SetFrom 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 the male genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the male genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of male external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of male external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of The Male Genitalia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Male Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Male External Genitalia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Male External Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal internal female genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal internal female genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent internal female genitalia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent internal female genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent internal female genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent internal female genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal internal female genitalia morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal internal female genitalia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
male genitalia development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male genitalia development biological process from the curated GO Biological Process Annotations 2015 dataset. |
male genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
hypoplastic male external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplastic male external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ambiguous genitalia, male Gene SetFrom HPO Gene-Disease Associations genes associated with the ambiguous genitalia, male phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent external male genitalia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent external male genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged external male genitalia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged external male genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external male genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small external male genitalia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small external male genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
external male genitalia atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Ambiguous Genitalia, Male Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ambiguous Genitalia, Male in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
male genitalia development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the male genitalia development biological process from the curated GO Biological Process Annotations 2023 dataset. |
external male genitalia atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent external male genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent external male genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal external male genitalia morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal external male genitalia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small external male genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small external male genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ambiguous external male genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ambiguous external male genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged external male genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged external male genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male genitalia morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male genitalia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
external male genitalia hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the external male genitalia hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male genitalia morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal male genitalia morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
absent external male genitalia Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the absent external male genitalia phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
male genitalia development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male genitalia development biological process from the curated GO Biological Process Annotations 2025 dataset. |
internal male genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue internal male genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
internal male genital organ Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue internal male genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
internal male genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue internal male genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Internal male genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Internal male genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal male genital organ Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Internal male genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal male genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Internal male genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom 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. |
functional respiratory abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional respiratory abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the functional respiratory abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
functional abnormality of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the functional abnormality of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
functional abnormality of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the functional abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
functional abnormality of the middle ear Gene SetFrom HPO Gene-Disease Associations genes associated with the functional abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the functional abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Functional Abnormality Of The Gastrointestinal Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Abnormality Of The Gastrointestinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Abnormality Of The Bladder Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Abnormality Of The Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormality of the female genitalia Gene SetFrom 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 female external genitalia Gene SetFrom 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 the female genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the female genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of Female External Genitalia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Female External Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
abnormality of the internal auditory canal Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the internal auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene SetFrom 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. |
ion channels and their functional role in vascular endothelium Gene SetFrom Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset. |
Functional Laterality Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Functional Laterality in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
functional diarrhea Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease functional diarrhea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
functional gastric disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease functional gastric disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
functional colonic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease functional colonic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
functional laterality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease functional laterality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
unexplained (functional) dyspepsia. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease unexplained (functional) dyspepsia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
functional differences Gene SetFrom GAD Gene-Disease Associations genes associated with the disease functional differences in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Functional MRI Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Functional MRI phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
functional motor problems Gene SetFrom HPO Gene-Disease Associations genes associated with the functional motor problems phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Hearing Loss, Functional Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Functional phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Colonic Diseases, Functional Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Colonic Diseases, Functional phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Functional Laterality Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Functional Laterality phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Triple functional domain protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Triple functional domain protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Catalase, mono-functional, haem-containing Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Catalase, mono-functional, haem-containing protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Catalase, mono-functional, haem-containing, clades 1 and 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Catalase, mono-functional, haem-containing, clades 1 and 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal functional residual capacity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal functional residual capacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Eye-lacrimal gland functional unit cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-lacrimal gland functional unit cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Functional Diarrhoea (Due To Spastic Colon) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Diarrhoea (Due To Spastic Colon) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Functional Gastrointestinal Disorders Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Gastrointestinal Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Functional Diarrhea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Constipation - Functional Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Constipation - Functional in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Functional Proteinuria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Proteinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colonic Diseases, Functional Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colonic Diseases, Functional in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Functional Neurological Symptom Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Neurological Symptom Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Functional Mitral Regurgitation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Mitral Regurgitation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Functional Disorder Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Disorder Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Functional Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Intestinal Obstruction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Motor Deficit Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Motor Deficit in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Hyposplenism Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Hyposplenism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Abdominal Pain Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Abdominal Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Laterality Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Laterality in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal functional residual capacity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal functional residual capacity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Functional myeloid cell_Brain_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Functional myeloid cell_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
EV release from cardiac cells and their functional effects Gene SetFrom WikiPathways Pathways 2024 proteins participating in the EV release from cardiac cells and their functional effects pathway from the WikiPathways Pathways 2024 dataset. |
Functional gastric disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Functional gastric disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Functional diarrhea Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Functional diarrhea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Functional colonic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Functional colonic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Functional motor deficit Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Functional motor deficit phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Rapid functional decline in sporadic amyotrophic lateral sclerosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Rapid functional decline in sporadic amyotrophic lateral sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Gut microbiota (functional units) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gut microbiota (functional units) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
3-month functional outcome in ischaemic stroke (modified Rankin score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the 3-month functional outcome in ischaemic stroke (modified Rankin score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
3-month functional outcome in non-lacunar ischaemic stroke (modified Rankin score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the 3-month functional outcome in non-lacunar ischaemic stroke (modified Rankin score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
3-month functional outcome in lacunar ischaemic stroke (modified Rankin score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the 3-month functional outcome in lacunar ischaemic stroke (modified Rankin score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Meningococcal C functional antibody titers post childhood immunization Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Meningococcal C functional antibody titers post childhood immunization phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Functional MRI Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Functional MRI phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Language functional connectivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Language functional connectivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
genitalia Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term genitalia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
external genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the external genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
female genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
female genitalia development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female genitalia development biological process from the curated GO Biological Process Annotations 2015 dataset. |
genitalia development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the genitalia development biological process from the curated GO Biological Process Annotations 2015 dataset. |
abnormal external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hypoplastic female external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplastic female external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the absent external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
gonadal tissue inappropriate for external genitalia or chromosomal sex Gene SetFrom HPO Gene-Disease Associations genes associated with the gonadal tissue inappropriate for external genitalia or chromosomal sex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
overgrowth of external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the overgrowth of external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ambiguous genitalia, female Gene SetFrom HPO Gene-Disease Associations genes associated with the ambiguous genitalia, female phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anteriorly displaced genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the anteriorly displaced genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
female external genitalia in individual with 46,xy karyotype Gene SetFrom HPO Gene-Disease Associations genes associated with the female external genitalia in individual with 46,xy karyotype phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ambiguous genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the ambiguous genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal female genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent external female genitalia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent external female genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external female genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external female genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hydranencephaly with abnormal genitalia Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydranencephaly with abnormal genitalia phenotype from the curated OMIM Gene-Disease Associations dataset. |
Ambiguous Genitalia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ambiguous Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal External Genitalia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal External Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hydranencephaly And Abnormal Genitalia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hydranencephaly And Abnormal Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ambiguous Genitalia, Female Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ambiguous Genitalia, Female in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female External Genitalia In Individual With 46,Xy Karyotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female External Genitalia In Individual With 46,Xy Karyotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Freckled Genitalia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Freckled Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent External Genitalia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent External Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Overgrowth Of External Genitalia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Overgrowth Of External Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anteriorly Displaced Genitalia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anteriorly Displaced Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Gonadal Tissue Inappropriate For External Genitalia Or Chromosomal Sex Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gonadal Tissue Inappropriate For External Genitalia Or Chromosomal Sex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
female genitalia development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the female genitalia development biological process from the curated GO Biological Process Annotations 2023 dataset. |
female genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the female genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
genitalia development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the genitalia development biological process from the curated GO Biological Process Annotations 2023 dataset. |
external genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the external genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
ambiguous external female genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ambiguous external female genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent external female genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent external female genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal external female genitalia morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal external female genitalia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female genitalia morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female genitalia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
female genitalia development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female genitalia development biological process from the curated GO Biological Process Annotations 2025 dataset. |
female genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
genitalia development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the genitalia development biological process from the curated GO Biological Process Annotations 2025 dataset. |
external genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the external genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
Corpus callosum agenesis-abnormal genitalia syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corpus callosum agenesis-abnormal genitalia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Methemoglobinemia and ambiguous genitalia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Methemoglobinemia and ambiguous genitalia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corpus callosum agenesis-abnormal genitalia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Corpus callosum agenesis-abnormal genitalia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ambiguous genitalia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ambiguous genitalia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
globus pallidus, internal segment, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in globus pallidus, internal segment, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
globus pallidus, internal segment, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in globus pallidus, internal segment, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
AOB, internal plexiform layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in AOB, internal plexiform layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Globus pallidus, internal segment Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Globus pallidus, internal segment relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
internal cortical nucleus of inferior colliculus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in internal cortical nucleus of inferior colliculus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
internal granular layer of CbHCx Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in internal granular layer of CbHCx relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
internal globus pallidus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in internal globus pallidus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
internal granular layer of CbVCx Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in internal granular layer of CbVCx relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
internal segment of globus pallidus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in internal segment of globus pallidus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
internal ribosome entry pathway Gene SetFrom Biocarta Pathways proteins participating in the internal ribosome entry pathway pathway from the Biocarta Pathways dataset. |
Carotid Artery, Internal Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Carotid Artery, Internal in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
internal hemorrhoid Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease internal hemorrhoid in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
carotid artery, internal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carotid artery, internal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carotid artery, internal, dissection; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carotid artery, internal, dissection; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carotid artery, internal, dissection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carotid artery, internal, dissection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
internal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term internal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
internal peptidyl-lysine acetylation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the internal peptidyl-lysine acetylation biological process from the curated GO Biological Process Annotations 2015 dataset. |
internal protein amino acid acetylation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the internal protein amino acid acetylation biological process from the curated GO Biological Process Annotations 2015 dataset. |
multivesicular body, internal vesicle lumen Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the multivesicular body, internal vesicle lumen cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
multivesicular body, internal vesicle Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the multivesicular body, internal vesicle cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
internal hemorrhage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the internal hemorrhage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
internal hemorrhage Gene SetFrom HPO Gene-Disease Associations genes associated with the internal hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dilatated internal auditory canal Gene SetFrom HPO Gene-Disease Associations genes associated with the dilatated internal auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of internal organs Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of internal organs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Carotid Artery, Internal, Dissection Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Carotid Artery, Internal, Dissection phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
absent brain internal capsule Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent brain internal capsule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal internal nares morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal internal nares morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
internal hemorrhage Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the internal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brain internal capsule size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brain internal capsule size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal internal auditory canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal internal auditory canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal internal carotid artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal internal carotid artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain internal capsule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain internal capsule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory bulb internal plexiform layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory bulb internal plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal internal anal sphincter morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal internal anal sphincter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
internal female genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue internal female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
internal female genital organ Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue internal female genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
internal plexiform layer Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue internal plexiform layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
internal female genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue internal female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
internal carotid artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue internal carotid artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
internal secretion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue internal secretion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
internal iliac artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue internal iliac artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Abnormal Internal Carotid Artery Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Internal Carotid Artery Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Internal Carotid Artery Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Internal Carotid Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Internal Lesion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Internal Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Internal Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Internal Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Internal Carotid Artery Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Internal Carotid Artery Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Carotid Artery, Internal, Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Carotid Artery, Internal, Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thrombosed Internal Hemorrhoids Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thrombosed Internal Hemorrhoids in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Duplication Of Internal Organs Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Duplication Of Internal Organs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Internal Carotid Artery Calcification Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Internal Carotid Artery Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Internal Ophthalmoplegia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Internal Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Narrow Internal Auditory Canal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Narrow Internal Auditory Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dilatated Internal Auditory Canal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dilatated Internal Auditory Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Internal Hemorrhage Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Internal Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Temporomandibular Joint Internal Derangement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Temporomandibular Joint Internal Derangement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intimal Medial Thickness Of Internal Carotid Artery, Modifier Of Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intimal Medial Thickness Of Internal Carotid Artery, Modifier Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anomalous Branches Of Internal Carotid Artery Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anomalous Branches Of Internal Carotid Artery in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
internal protein amino acid acetylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the internal protein amino acid acetylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
internal peptidyl-lysine acetylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the internal peptidyl-lysine acetylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
multivesicular body, internal vesicle lumen Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the multivesicular body, internal vesicle lumen cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
multivesicular body, internal vesicle Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the multivesicular body, internal vesicle cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
internal hemorrhage Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the internal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal olfactory bulb internal plexiform layer morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory bulb internal plexiform layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal internal anal sphincter morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal internal anal sphincter morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brain internal capsule size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain internal capsule size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain internal capsule morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain internal capsule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal internal carotid artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal internal carotid artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal internal auditory canal morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal internal auditory canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent brain internal capsule Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent brain internal capsule phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal internal nares morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal internal nares morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal long bone internal diameter Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone internal diameter phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
anastomosis between internal carotid artery and basilar artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the anastomosis between internal carotid artery and basilar artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent parasellar internal carotid artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent parasellar internal carotid artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal internal carotid artery topology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal internal carotid artery topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent canalicular internal carotid artery segment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent canalicular internal carotid artery segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased internal diameter of femur Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased internal diameter of femur phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased internal diameter of femur Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased internal diameter of femur phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal parasellar internal carotid artery branch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal parasellar internal carotid artery branch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
internal protein amino acid acetylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the internal protein amino acid acetylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
internal peptidyl-lysine acetylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the internal peptidyl-lysine acetylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
mitophagy by internal vacuole formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mitophagy by internal vacuole formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
multivesicular body, internal vesicle lumen Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the multivesicular body, internal vesicle lumen cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
multivesicular body, internal vesicle Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the multivesicular body, internal vesicle cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
internal N(7)-methylguanine-containing RNA reader activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the internal N(7)-methylguanine-containing RNA reader activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
internal mRNA (guanine-N7-)-methyltransferase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the internal mRNA (guanine-N7-)-methyltransferase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Internal hemorrhoid Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Internal hemorrhoid in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central nervous system tumor with BCOR internal tandem duplication Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system tumor with BCOR internal tandem duplication in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Internal hordeolum Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Internal hordeolum in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Internal auditory canal meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Internal auditory canal meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Total internal ophthalmoplegia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Total internal ophthalmoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Internal auditory canal lipoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Internal auditory canal lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Internal female genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Internal female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal female genital organ Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Internal female genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal female genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Internal female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal carotid artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Internal carotid artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal capsule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Internal capsule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal iliac artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Internal iliac artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal plexiform layer Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Internal plexiform layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal secretion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Internal secretion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Multivesicular body, internal vesicle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Multivesicular body, internal vesicle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Multivesicular body, internal vesicle lumen Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Multivesicular body, internal vesicle lumen cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Multivesicular body, internal vesicle lumen Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Multivesicular body, internal vesicle lumen cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Multivesicular body, internal vesicle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Multivesicular body, internal vesicle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Left ventricle diastolic internal dimension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricle diastolic internal dimension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Carotid artery internal diameter Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Carotid artery internal diameter phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left ventricular internal dimension in diastole Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular internal dimension in diastole phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left ventricular internal dimension in systole Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular internal dimension in systole phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Male hypogonadism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Male hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
CATSPER-Related Male Infertility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the CATSPER-Related Male Infertility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
male pronucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the male pronucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
male germ cell nucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the male germ cell nucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
male pronucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the male pronucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
male germ cell nucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the male germ cell nucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Male Urogenital Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Male Urogenital Diseases from the curated CTD Gene-Disease Associations dataset. |
Infertility, Male Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Infertility, Male from the curated CTD Gene-Disease Associations dataset. |
Genital Diseases, Male Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Genital Diseases, Male from the curated CTD Gene-Disease Associations dataset. |
Breast Neoplasms, Male Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Breast Neoplasms, Male from the curated CTD Gene-Disease Associations dataset. |
Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa from the curated CTD Gene-Disease Associations dataset. |
Deafness, Sensorineural, And Male Infertility Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Sensorineural, And Male Infertility from the curated CTD Gene-Disease Associations dataset. |
Infertility, Male Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Infertility, Male in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
male reproductive system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease male reproductive system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
male infertility Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease male infertility in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
male reproductive system disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease male reproductive system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
male reproductive organ cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease male reproductive organ cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
male reproductive organ benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease male reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
male urethral cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease male urethral cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
male reproductive organ cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease male reproductive organ cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
male infertility Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease male infertility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
male breast cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease male breast cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
male reproductive system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease male reproductive system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cystic fibrosis; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
male-pattern baldness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease male-pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; urogenital abnormalities Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; urogenital abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
female preferences for male odors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease female preferences for male odors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; sex chromosome aberrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; oligospermia; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; oligospermia; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nonsurvivors of sepsis (male only) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nonsurvivors of sepsis (male only) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dna damage; infertility, male; varicocele Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dna damage; infertility, male; varicocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; breast neoplasms, male; mammary neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult male height Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult male height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome deletion; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome deletion; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dna damage; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dna damage; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cryptorchidism; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cryptorchidism; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; neoplasms, prostatic; neoplasms, testis; prostatic neoplasms; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; neoplasms, prostatic; neoplasms, testis; prostatic neoplasms; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
male longevity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease male longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial male-limited precocious puberty. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial male-limited precocious puberty. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthenozoospermia; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthenozoospermia; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
testosterone; infertility, male; hypogonadism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease testosterone; infertility, male; hypogonadism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gonadal dysgenesis, 46,xy; infertility, male; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gonadal dysgenesis, 46,xy; infertility, male; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms; ovarian neoplasm; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; varicocele Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; varicocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; hypospadias; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; hypospadias; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
male breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease male breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; breast neoplasms, male; mammary neoplasms; ovarian neoplasm; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
wilms' tumor and congenital male genitourinary malformation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease wilms' tumor and congenital male genitourinary malformation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
male infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease male infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced trans-activation impaired sperm production and male infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced trans-activation impaired sperm production and male infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
male pattern baldness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease male pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovaries and premature male pattern baldness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovaries and premature male pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms, prostatic; ovarian neoplasm; ovarian neoplasms; prostatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms, prostatic; ovarian neoplasm; ovarian neoplasms; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; sertoli cell-only syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; sertoli cell-only syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hernia, inguinal; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hernia, inguinal; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
male-to-female transsexualism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease male-to-female transsexualism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
left ventricular mass in male athletes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease left ventricular mass in male athletes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; oligospermia; sex chromosome aberrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; oligospermia; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
male Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term male in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
POR_DELETION_GDS1093_240_mouse_Liver from male 3 month old Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the POR_DELETION_GDS1093_240_mouse_Liver from male 3 month old gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
male gamete generation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male gamete generation biological process from the curated GO Biological Process Annotations 2015 dataset. |
male courtship behavior Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male courtship behavior biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of male germ cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of male germ cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
development of secondary male sexual characteristics Gene SetFrom GO Biological Process Annotations 2015 genes participating in the development of secondary male sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset. |
male germ cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male germ cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of male germ cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of male germ cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
male meiosis i Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male meiosis i biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of male gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of male gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
male germ-line sex determination Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male germ-line sex determination biological process from the curated GO Biological Process Annotations 2015 dataset. |
male pronucleus assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male pronucleus assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
dna demethylation of male pronucleus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the dna demethylation of male pronucleus biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of male germ cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of male germ cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
male sex differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male sex differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
male sex determination Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male sex determination biological process from the curated GO Biological Process Annotations 2015 dataset. |
male anatomical structure morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male anatomical structure morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of male gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of male gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
male meiosis chromosome segregation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male meiosis chromosome segregation biological process from the curated GO Biological Process Annotations 2015 dataset. |
male meiosis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male meiosis biological process from the curated GO Biological Process Annotations 2015 dataset. |
male meiosis chromosome separation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male meiosis chromosome separation biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of male gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of male gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
inter-male aggressive behavior Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inter-male aggressive behavior biological process from the curated GO Biological Process Annotations 2015 dataset. |
male germ-line stem cell asymmetric division Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male germ-line stem cell asymmetric division biological process from the curated GO Biological Process Annotations 2015 dataset. |
male gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
male mating behavior Gene SetFrom GO Biological Process Annotations 2015 genes participating in the male mating behavior biological process from the curated GO Biological Process Annotations 2015 dataset. |
male pronucleus Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the male pronucleus cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
male germ cell nucleus Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the male germ cell nucleus cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
Male-pattern baldness Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Male-pattern baldness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Male infertility Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Male infertility phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Breast cancer (male) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Breast cancer (male) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
male infertility Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease male infertility in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
male reproductive system disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease male reproductive system disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
male reproductive organ cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease male reproductive organ cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
male infertility Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the male infertility phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
male hypogonadism Gene SetFrom HPO Gene-Disease Associations genes associated with the male hypogonadism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
gonadal dysgenesis, male Gene SetFrom HPO Gene-Disease Associations genes associated with the gonadal dysgenesis, male phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
male infertility Gene SetFrom HPO Gene-Disease Associations genes associated with the male infertility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
male pseudohermaphroditism Gene SetFrom HPO Gene-Disease Associations genes associated with the male pseudohermaphroditism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Genital Neoplasms, Male Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genital Neoplasms, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Infertility, Male Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Infertility, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Genital Diseases, Male Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genital Diseases, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Breast Neoplasms, Male Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Breast Neoplasms, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Male Urogenital Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Male Urogenital Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
DMRT/protein doublesex/protein male abnormal 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Male sterility, NAD-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Male sterility, NAD-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Male enhanced antigen 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Male enhanced antigen 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein male abnormal 21-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein male abnormal 21-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein male-specific lethal-1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein male-specific lethal-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Transcription factor homeodomain, male germ-cell Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Transcription factor homeodomain, male germ-cell protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal male urethra morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male germ cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male germ cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced male fertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced male fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male preputial gland morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male preputial gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed male fertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed male fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small male preputial glands Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small male preputial glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive system morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male prostatic urethra morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male prostatic urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced male mating frequency Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced male mating frequency phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent male inguinal canal Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent male inguinal canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent male preputial gland Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent male preputial gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male accessory sex gland morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male accessory sex gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
submission towards male mice Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the submission towards male mice phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male inguinal canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male inguinal canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
male infertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the male infertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
arrest of male meiosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the arrest of male meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male meiosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
male pseudohermaphroditism Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the male pseudohermaphroditism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased male germ cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased male germ cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male germ cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male germ cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive gland morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal x-y chromosome synapsis during male meiosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal x-y chromosome synapsis during male meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{male germ cell tumor, somatic}, 273300, Gene SetFrom OMIM Gene-Disease Associations genes associated with the {male germ cell tumor, somatic}, 273300, phenotype from the curated OMIM Gene-Disease Associations dataset. |
{breast cancer, male, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {breast cancer, male, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
precocious puberty, male Gene SetFrom OMIM Gene-Disease Associations genes associated with the precocious puberty, male phenotype from the curated OMIM Gene-Disease Associations dataset. |
male germ cell tumor Gene SetFrom OMIM Gene-Disease Associations genes associated with the male germ cell tumor phenotype from the curated OMIM Gene-Disease Associations dataset. |
?male pseudohermaphroditism due to defective lh Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?male pseudohermaphroditism due to defective lh phenotype from the curated OMIM Gene-Disease Associations dataset. |
pseudohermaphroditism, male, with gynecomastia Gene SetFrom OMIM Gene-Disease Associations genes associated with the pseudohermaphroditism, male, with gynecomastia phenotype from the curated OMIM Gene-Disease Associations dataset. |
?male infertility Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?male infertility phenotype from the curated OMIM Gene-Disease Associations dataset. |
deafness and male infertility Gene SetFrom OMIM Gene-Disease Associations genes associated with the deafness and male infertility phenotype from the curated OMIM Gene-Disease Associations dataset. |
?male infertility due to acrosin deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?male infertility due to acrosin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
male Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term male in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Fetal Brain Male Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Fetal Brain Male relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Skeletal Muscle Male Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Skeletal Muscle Male relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Male Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells G-CSF-mobilized Male relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
male reproductive system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue male reproductive system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
external male genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue external male genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
male reproductive gland Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue male reproductive gland from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
male reproductive gland Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue male reproductive gland in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
male reproductive system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue male reproductive system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
external male genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue external male genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
male cone Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue male cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
male reproductive system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue male reproductive system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
male urethra Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue male urethra in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
male reproductive gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue male reproductive gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Klinefelter'S Syndrome - Male With More Than Two X Chromosomes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Klinefelter'S Syndrome - Male With More Than Two X Chromosomes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Pseudohermaphroditism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Pseudohermaphroditism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Pseudohermaphroditism: Deficiency Of Testicular 17,20-Desmolase Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Pseudohermaphroditism: Deficiency Of Testicular 17,20-Desmolase in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Carcinoma Of Male Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Carcinoma Of Male Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Epispadias, Male (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Epispadias, Male (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Infertility With Teratozoospermia Due To Single Gene Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Infertility With Teratozoospermia Due To Single Gene Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Infertility With Large-Headed, Multiflagellar, Polyploid Spermatozoa Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Infertility With Large-Headed, Multiflagellar, Polyploid Spermatozoa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Germ Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Germ Cell Tumor, Somatic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Germ Cell Tumor, Somatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Breast Cancer, Familial Male Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Breast Cancer, Familial Male in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Accessory Gland Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Accessory Gland Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Male Sexual Function Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Male Sexual Function in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Sexual Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Leydig Cell Adenoma, Somatic, With Male-Limited Precocious Puberty Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Leydig Cell Adenoma, Somatic, With Male-Limited Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Incomplete Male Pseudohermaphroditism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Incomplete Male Pseudohermaphroditism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Incomplete Male Pseudohermaphroditism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Incomplete Male Pseudohermaphroditism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Male Infertility Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Male Infertility in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Infertility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Male Infertility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Male Sterility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Male Sterility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Subfertility, Male Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subfertility, Male in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Male Puberty Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Male Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Male Germ Cell Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Male Germ Cell Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
male gonad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the male gonad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
male meiosis I Gene SetFrom GO Biological Process Annotations 2023 genes participating in the male meiosis I biological process from the curated GO Biological Process Annotations 2023 dataset. |
DNA demethylation of male pronucleus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the DNA demethylation of male pronucleus biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of male gonad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of male gonad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
male germ-line sex determination Gene SetFrom GO Biological Process Annotations 2023 genes participating in the male germ-line sex determination biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of male gonad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of male gonad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
development of primary male sexual characteristics Gene SetFrom GO Biological Process Annotations 2023 genes participating in the development of primary male sexual characteristics biological process from the curated GO Biological Process Annotations 2023 dataset. |
male gamete generation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the male gamete generation biological process from the curated GO Biological Process Annotations 2023 dataset. |
male meiosis chromosome separation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the male meiosis chromosome separation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of male germ cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of male germ cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of male germ cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of male germ cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
male germ-line stem cell asymmetric division Gene SetFrom GO Biological Process Annotations 2023 genes participating in the male germ-line stem cell asymmetric division biological process from the curated GO Biological Process Annotations 2023 dataset. |
male germ cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the male germ cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of male gonad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of male gonad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
male pronucleus Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the male pronucleus cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
male germ cell nucleus Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the male germ cell nucleus cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
reduced male fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced male fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced male mating frequency Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced male mating frequency phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
submission towards male mice Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the submission towards male mice phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male reproductive system morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male reproductive system morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
male infertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the male infertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased aggression towards male mice Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased aggression towards male mice phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male meiosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male meiosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased male germ cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased male germ cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male germ cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male germ cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
arrest of male meiosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the arrest of male meiosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased male germ cell apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased male germ cell apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
multinucleated giant male germ cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the multinucleated giant male germ cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent male preputial gland Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent male preputial gland phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased aggression towards male mice Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased aggression towards male mice phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male reproductive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male reproductive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
male pseudohermaphroditism Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the male pseudohermaphroditism phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed male fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed male fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male preputial gland morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male preputial gland morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small male preputial gland Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small male preputial gland phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male germ cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male germ cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male germ cell apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male germ cell apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male prostatic urethra morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male prostatic urethra morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent male inguinal canal Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent male inguinal canal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enhanced male fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced male fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal X-Y chromosome synapsis during male meiosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal X-Y chromosome synapsis during male meiosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal male accessory sex gland morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal male accessory sex gland morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal X-Y chromosome synaptonemal complex assembly during male meiosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal X-Y chromosome synaptonemal complex assembly during male meiosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
male infertility Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the male infertility phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Male infertility Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Male infertility pathway from the WikiPathways Pathways 2024 dataset. |
Male steroid hormones in cardiomyocyte energy metabolism Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Male steroid hormones in cardiomyocyte energy metabolism pathway from the WikiPathways Pathways 2024 dataset. |
Replacement of protamines by nucleosomes in the male pronucleus Gene Setproteins participating in the Replacement of protamines by nucleosomes in the male pronucleus pathway from the Reactome Pathways 2024 dataset. |
male meiosis chromosome segregation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male meiosis chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset. |
male gonad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male gonad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
male meiosis I Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male meiosis I biological process from the curated GO Biological Process Annotations 2025 dataset. |
epigenetic programing of male pronucleus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the epigenetic programing of male pronucleus biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of male gonad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of male gonad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
male germ-line sex determination Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male germ-line sex determination biological process from the curated GO Biological Process Annotations 2025 dataset. |
male meiotic nuclear division Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male meiotic nuclear division biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of male gonad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of male gonad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
male pronucleus assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male pronucleus assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
development of primary male sexual characteristics Gene SetFrom GO Biological Process Annotations 2025 genes participating in the development of primary male sexual characteristics biological process from the curated GO Biological Process Annotations 2025 dataset. |
male gamete generation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male gamete generation biological process from the curated GO Biological Process Annotations 2025 dataset. |
male meiosis chromosome separation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male meiosis chromosome separation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of male germ cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of male germ cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of male germ cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of male germ cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
male germ-line stem cell asymmetric division Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male germ-line stem cell asymmetric division biological process from the curated GO Biological Process Annotations 2025 dataset. |
male germ cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male germ cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
male meiosis cytokinesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the male meiosis cytokinesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of male gonad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of male gonad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
male pronucleus Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the male pronucleus cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
male germ cell nucleus Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the male germ cell nucleus cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Male reproductive system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Male reproductive system disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Male reproductive organ cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Male reproductive organ cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Male infertility Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Male infertility from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Familial male-limited precocious puberty Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial male-limited precocious puberty from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Male infertility due to globozoospermia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Male infertility due to globozoospermia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Male reproductive organ cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Male reproductive organ cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male reproductive system disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Male reproductive system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male breast cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Male breast cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male infertility Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Male infertility in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male reproductive system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male reproductive system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male reproductive organ cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male reproductive organ cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male infertility due to globozoospermia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male infertility due to globozoospermia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male infertility Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male infertility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male infertility due to acephalic spermatozoa Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male infertility due to acephalic spermatozoa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male reproductive organ benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male breast cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male breast cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial male-limited precocious puberty Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial male-limited precocious puberty in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male urethral cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male urethral cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Inhibited male orgasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inhibited male orgasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male reproductive system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Male reproductive system from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Male reproductive gland Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Male reproductive gland from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
External male genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue External male genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Male reproductive system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Male reproductive system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Male reproductive gland Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Male reproductive gland in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Male reproductive system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Male reproductive system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Male reproductive gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Male reproductive gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
External male genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue External male genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Male urethra Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Male urethra in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Male inflorescence Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Male inflorescence in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Male cone Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Male cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Male germ cell nucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Male germ cell nucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Male pronucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Male pronucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Male pronucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Male pronucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Male germline ring canal Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Male germline ring canal cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Male germ cell nucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Male germ cell nucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Male infertility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Male infertility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Male subfertility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Male subfertility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Carcinoma of male breast Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Carcinoma of male breast phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Male infertility due to gonadal dysgenesis or sperm disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Male infertility due to gonadal dysgenesis or sperm disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Male-pattern baldness Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Male-pattern baldness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Facial attractiveness (male raters) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Facial attractiveness (male raters) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer (male) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer (male) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Male fertility Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Male fertility phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Male infertility Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Male infertility phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Male sexual orientation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Male sexual orientation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom 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 SetFrom 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 SetFrom DISEASES Curated Gene-Disease Association 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 SetFrom DISEASES Text-mining Gene-Disease Association 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 SetFrom DISEASES Text-mining Gene-Disease Association 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 SetFrom DISEASES Text-mining Gene-Disease Association 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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; leiomyoma; radiation injuries; uterine neoplasms Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 upper limb bone Gene SetFrom 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 aortic valve Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 upper urinary tract Gene SetFrom 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 iris Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 musculature Gene SetFrom 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 cerebral white matter Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the face Gene SetFrom 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 facial skeleton Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 upper limb Gene SetFrom 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 the cerebral vasculature Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone mineral density Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 the curvature of the cornea Gene SetFrom 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 SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the metaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gastrointestinal tract Gene SetFrom 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 SetFrom 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 the hypothalamus-pituitary axis Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 upper limb metaphysis Gene SetFrom 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 metabolism/homeostasis Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 upper arm Gene SetFrom 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 ulna Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 humerus Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 body height Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 upper lip Gene SetFrom 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 the middle phalanx of the 5th finger Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 upper limb bone Gene SetFrom 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 thumb phalanx Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 musculature of the upper limbs Gene SetFrom 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 anterior chamber Gene SetFrom 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 SetFrom 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 SetFrom 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 the upper limb Gene SetFrom 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 binocular vision Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |