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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 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. |
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. |
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. |
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. |
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. |
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. |
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 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 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. |
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 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 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 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 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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
external female genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue external female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
external female genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue external female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
External female genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue External female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
External female genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue External female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
chlamydia infections; genital diseases, female; infertility, female; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chlamydia infections; genital diseases, female; infertility, female; inflammation in GWAS and other genetic association datasets from the GAD 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. |
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. |
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. |
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. |
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 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. |
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 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 the external nose Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the external nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations 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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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, external segment, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in globus pallidus, external segment, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
globus pallidus, external segment, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in globus pallidus, external segment, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
external globus pallidum Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in external globus pallidum relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
r9 part of external cuneate nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r9 part of external cuneate nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
external part of AOD Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in external part of AOD relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
external part of AOV Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in external part of AOV relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Inferior colliculus, external nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Inferior colliculus, external nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
r10 part of external cuneate nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r10 part of external cuneate nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Parabrachial nucleus, medial division, external medial part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Parabrachial nucleus, medial division, external medial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
external cortical nucleus of inferior colliculus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in external cortical nucleus of inferior colliculus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Anterior olfactory nucleus, external part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior olfactory nucleus, external part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
External cuneate nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in External cuneate nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
bed nucleus of the external capsule Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in bed nucleus of the external capsule relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Globus pallidus, external segment Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Globus pallidus, external segment relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Parabrachial nucleus, lateral division, external lateral part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Parabrachial nucleus, lateral division, external lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
external granular (germinal) layer of upper rhombic lip Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in external granular (germinal) layer of upper rhombic lip relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
external granular (germinal) layer of lower rhombic lip Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in external granular (germinal) layer of lower rhombic lip relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
external segment of globus pallidus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in external segment of globus pallidus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Minicore myopathy with external ophthalmoplegia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Minicore myopathy with external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
extrinsic component of external side of plasma membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the extrinsic component of external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
anchored component of external side of plasma membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the anchored component of external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
intrinsic component of external side of plasma membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the intrinsic component of external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
external side of cell outer membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the external side of cell outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
external encapsulating structure Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the external encapsulating structure cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
integral component of external side of plasma membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the integral component of external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
external side of plasma membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
external encapsulating structure part Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the external encapsulating structure part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
external encapsulating structure Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the external encapsulating structure cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
external side of plasma membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the external side of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
endospore external encapsulating structure Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the endospore external encapsulating structure cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
external encapsulating structure part Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the external encapsulating structure part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset. |
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 from the curated CTD Gene-Disease Associations dataset. |
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 from the curated CTD Gene-Disease Associations dataset. |
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 from the curated CTD Gene-Disease Associations dataset. |
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset. |
Minicore Myopathy with External Ophthalmoplegia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Minicore Myopathy with External Ophthalmoplegia from the curated CTD Gene-Disease Associations dataset. |
Ophthalmoplegia, Chronic Progressive External Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ophthalmoplegia, Chronic Progressive External from the curated CTD Gene-Disease Associations dataset. |
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 from the curated CTD Gene-Disease Associations dataset. |
Ophthalmoplegia, External, and Myopia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ophthalmoplegia, External, and Myopia from the curated CTD Gene-Disease Associations dataset. |
Ear, External Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Ear, External in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
chronic progressive external ophthalmoplegia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease chronic progressive external ophthalmoplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
external ear cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease external ear cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
external ear disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease external ear disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chronic progressive external ophthalmoplegia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic progressive external ophthalmoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
external ear carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease external ear carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ophthalmoplegia, chronic progressive external Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ophthalmoplegia, chronic progressive external in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
progressive external ophthalmoplegia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease progressive external ophthalmoplegia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
external Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term external in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
external encapsulating structure organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the external encapsulating structure organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
cell proliferation in external granule layer Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cell proliferation in external granule layer biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of external stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of external stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of response to external stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of response to external stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of external biotic stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of external biotic stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to external stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to external stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of response to external stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of response to external stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to external biotic stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to external biotic stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to external stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to external stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of response to external stimulus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of response to external stimulus biological process from the curated GO Biological Process Annotations 2015 dataset. |
extrinsic component of external side of plasma membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the extrinsic component of external side of plasma membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
intrinsic component of external side of plasma membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the intrinsic component of external side of plasma membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
external side of cell outer membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the external side of cell outer membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
external encapsulating structure Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the external encapsulating structure cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
integral component of external side of plasma membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the integral component of external side of plasma membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
anchored component of external side of plasma membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the anchored component of external side of plasma membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
external side of plasma membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the external side of plasma membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
external encapsulating structure part Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the external encapsulating structure part cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
displacement of the external urethral meatus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the displacement of the external urethral meatus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
external ear malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the external ear malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
nonprogressive restrictive external ophthalmoplegia Gene SetFrom HPO Gene-Disease Associations genes associated with the nonprogressive restrictive external ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
displacement of the external urethral meatus Gene SetFrom HPO Gene-Disease Associations genes associated with the displacement of the external urethral meatus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
external ophthalmoplegia Gene SetFrom HPO Gene-Disease Associations genes associated with the external ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
restrictive external ophthalmoplegia Gene SetFrom HPO Gene-Disease Associations genes associated with the restrictive external ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
external genital hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the external genital hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive external ophthalmoplegia Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive external ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atresia of the external auditory canal Gene SetFrom HPO Gene-Disease Associations genes associated with the atresia of the external auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
exostosis of the external auditory canal Gene SetFrom HPO Gene-Disease Associations genes associated with the exostosis of the external auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the external ear Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the external ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
stenosis of the external auditory canal Gene SetFrom HPO Gene-Disease Associations genes associated with the stenosis of the external auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Ophthalmoplegia, Chronic Progressive External Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Ophthalmoplegia, Chronic Progressive External phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal external urethral orifice morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external urethral orifice morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum external granule cell layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum external granule cell layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external nares morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external nares morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external auditory canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external auditory canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external carotid artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external carotid artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent external auditory canal Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent external auditory canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory bulb external plexiform layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory bulb external plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thin external granule cell layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thin external granule cell layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
progressive external ophthalmoplegia, autosomal dominant, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal dominant, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
progressive external ophthalmoplegia, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
minicore myopathy with external ophthalmoplegia Gene SetFrom OMIM Gene-Disease Associations genes associated with the minicore myopathy with external ophthalmoplegia phenotype from the curated OMIM Gene-Disease Associations dataset. |
progressive external ophthalmoplegia with mitochondrial dna deletions 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
progressive external ophthalmoplegia, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations 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. |
external iliac artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue external iliac artery in abstracts of biomedical publications from the TISSUES Text-mining 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. |
external carotid artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue external carotid artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
external gill Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue external gill in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
external plexiform layer Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue external plexiform layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
External Exotoses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease External Exotoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Progressive External Ophthalmoplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Progressive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Minicore Myopathy With External Ophthalmoplegia (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Minicore Myopathy With External Ophthalmoplegia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
External Carotid Artery Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease External Carotid Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
External Ophthalmoplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Absence Of External Ear Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of External Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Exostosis Of External Ear Canal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Exostosis Of External Ear Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
External Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease External Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
External Auditory Canal, Bilateral Atresia Of, With Congenital Vertical Talus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease External Auditory Canal, Bilateral Atresia Of, With Congenital Vertical Talus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive External Ophthalmoplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
External Carotid Artery Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease External Carotid Artery Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
External Resorption Of Tooth Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease External Resorption Of Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Displacement Of The External Urethral Meatus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Displacement Of The External Urethral Meatus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Absence, Atresia And Stricture Of Auditory Canal (External) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence, Atresia And Stricture Of Auditory Canal (External) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nonprogressive Restrictive External Ophthalmoplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nonprogressive Restrictive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
External Genital Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype External Genital Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The External Ear Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The External Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bilateral External Ear Deformity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bilateral External Ear Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Restrictive External Ophthalmoplegia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Restrictive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
regulation of response to external stimulus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of response to external stimulus biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of response to external stimulus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of response to external stimulus biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of response to external stimulus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of response to external stimulus biological process from the curated GO Biological Process Annotations 2023 dataset. |
external encapsulating structure organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the external encapsulating structure organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
detection of external biotic stimulus Gene SetFrom GO Biological Process Annotations 2023 genes participating in the detection of external biotic stimulus biological process from the curated GO Biological Process Annotations 2023 dataset. |
cell proliferation in external granule layer Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cell proliferation in external granule layer biological process from the curated GO Biological Process Annotations 2023 dataset. |
extrinsic component of external side of plasma membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the extrinsic component of external side of plasma membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
external side of apical plasma membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the external side of apical plasma membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
absent external auditory canal Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent external auditory canal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cerebellum external granule cell layer morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum external granule cell layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal external auditory canal morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal external auditory canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal olfactory bulb external plexiform layer morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory bulb external plexiform layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent external nares Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent external nares phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin external granule cell layer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin external granule cell layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small external nares Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small external nares phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal external nares morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal external nares morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
external auditory canal stenosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the external auditory canal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal external carotid artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal external carotid artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
single external naris Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the single external naris phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brain external capsule size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brain external capsule size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal external carotid artery origin Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal external carotid artery origin phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
regulation of response to external stimulus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of response to external stimulus biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of response to external stimulus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of response to external stimulus biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of response to external stimulus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of response to external stimulus biological process from the curated GO Biological Process Annotations 2025 dataset. |
external encapsulating structure organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the external encapsulating structure organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
detection of external biotic stimulus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of external biotic stimulus biological process from the curated GO Biological Process Annotations 2025 dataset. |
cell proliferation in external granule layer Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cell proliferation in external granule layer biological process from the curated GO Biological Process Annotations 2025 dataset. |
external side of apical plasma membrane Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the external side of apical plasma membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
extrinsic component of external side of plasma membrane Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the extrinsic component of external side of plasma membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Chronic progressive external ophthalmoplegia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chronic progressive external ophthalmoplegia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Chronic progressive external ophthalmoplegia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic progressive external ophthalmoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
External ear disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease External ear disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
External ear squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease External ear squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
External ear carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease External ear carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
External ear basal cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease External ear basal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
External ear cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease External ear cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation 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. |
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. |
External ectoderm Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue External ectoderm in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
External carotid artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue External carotid artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
External plexiform layer Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue External plexiform layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
External iliac artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue External iliac artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
External gill Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue External gill in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
External side of plasma membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the External side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
External encapsulating structure Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the External encapsulating structure cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Extrinsic component of external side of plasma membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Extrinsic component of external side of plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
External side of apical plasma membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the External side of apical plasma membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
External encapsulating structure Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the External encapsulating structure cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Endospore external encapsulating structure Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Endospore external encapsulating structure cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Integral component of external side of plasma membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Integral component of external side of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
External side of cell wall Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the External side of cell wall cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
External side of cell outer membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the External side of cell outer membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
External side of apical plasma membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the External side of apical plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Intrinsic component of external side of cell outer membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Intrinsic component of external side of cell outer membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Anchored component of external side of plasma membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Anchored component of external side of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
External side of plasma membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the External side of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Extrinsic component of external side of plasma membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Extrinsic component of external side of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Intrinsic component of external side of plasma membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Intrinsic component of external side of plasma membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Progressive external ophthalmoplegia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive progressive external ophthalmoplegia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Carotid artery external diameter Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Carotid artery external diameter phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
female germ cell nucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the female germ cell nucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
female pronucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the female pronucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
female germline ring canal Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the female germline ring canal cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
female germline ring canal inner rim Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the female germline ring canal inner rim cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
female germ cell nucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the female germ cell nucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
female pronucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the female pronucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Infertility, Female Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Infertility, Female from the curated CTD Gene-Disease Associations dataset. |
Genital Neoplasms, Female Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Genital Neoplasms, Female from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, Female-Restricted, with Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Female-Restricted, with Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Female Urogenital Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Female Urogenital Diseases from the curated CTD Gene-Disease Associations dataset. |
Genital Diseases, Female Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Genital Diseases, Female from the curated CTD Gene-Disease Associations dataset. |
female reproductive system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease female reproductive system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
female reproductive organ cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease female reproductive organ cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
female reproductive organ benign neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease female reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
female reproductive system disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease female reproductive system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
female urethral cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female urethral cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female breast cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female breast cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female stress incontinence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female stress incontinence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female reproductive system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female reproductive system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female reproductive organ cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female reproductive organ cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female breast carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female breast carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female reproductive organ benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
prolapse of female genital organ Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease prolapse of female genital organ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female reproductive endometrioid cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female reproductive endometrioid cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 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. |
infertility, female; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; pof - premature ovarian failure; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; ovarian failure, premature Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; ovarian failure, premature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anovulation; infertility, female; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anovulation; infertility, female; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
female infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease female infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chlamydia infections; genital diseases, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chlamydia infections; genital diseases, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female 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. |
abortion, habitual; activated protein c resistance; infertility, female; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; infertility, female; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
postnatal female survival Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postnatal female survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; infertility, female; ovarian cyst, nos; ovarian cysts Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; ovarian cyst, nos; ovarian cysts in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; embryo loss; infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; embryo loss; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chlamydia infections; infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chlamydia infections; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genital diseases, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genital diseases, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genital neoplasms, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genital neoplasms, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
female pseudohermaphroditism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease female pseudohermaphroditism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chlamydia infections; fallopian tube diseases; infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chlamydia infections; fallopian tube diseases; infertility, female 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. |
breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
female Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term female in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
development of primary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2015 genes participating in the development of primary female sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset. |
female pregnancy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female pregnancy biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic process involved in female pregnancy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic process involved in female pregnancy biological process from the curated GO Biological Process Annotations 2015 dataset. |
female meiosis sister chromatid cohesion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female meiosis sister chromatid cohesion biological process from the curated GO Biological Process Annotations 2015 dataset. |
female pronucleus assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female pronucleus assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
female meiosis i Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female meiosis i biological process from the curated GO Biological Process Annotations 2015 dataset. |
maternal process involved in female pregnancy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the maternal process involved in female pregnancy biological process from the curated GO Biological Process Annotations 2015 dataset. |
female gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
female somatic sex determination Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female somatic sex determination biological process from the curated GO Biological Process Annotations 2015 dataset. |
female meiotic division Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female meiotic division biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of female receptivity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of female receptivity biological process from the curated GO Biological Process Annotations 2015 dataset. |
female mating behavior Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female mating behavior biological process from the curated GO Biological Process Annotations 2015 dataset. |
development of secondary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2015 genes participating in the development of secondary female sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of female gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
female courtship behavior Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female courtship behavior biological process from the curated GO Biological Process Annotations 2015 dataset. |
protection of dna demethylation of female pronucleus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protection of dna demethylation of female pronucleus biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of female gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
female meiosis ii Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female meiosis ii biological process from the curated GO Biological Process Annotations 2015 dataset. |
spindle assembly involved in female meiosis i Gene SetFrom GO Biological Process Annotations 2015 genes participating in the spindle assembly involved in female meiosis i biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of female receptivity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of female receptivity biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of female receptivity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of female receptivity biological process from the curated GO Biological Process Annotations 2015 dataset. |
female gamete generation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female gamete generation biological process from the curated GO Biological Process Annotations 2015 dataset. |
female sex determination Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female sex determination biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of female gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
spindle assembly involved in female meiosis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the spindle assembly involved in female meiosis biological process from the curated GO Biological Process Annotations 2015 dataset. |
female germ cell nucleus Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the female germ cell nucleus cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
female pronucleus Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the female pronucleus cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
Sexual dysfunction (female) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Sexual dysfunction (female) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
prolapse of female genital organ Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease prolapse of female genital organ in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
female breast cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease female breast cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
female reproductive organ cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease female reproductive organ cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
female reproductive organ benign neoplasm Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease female reproductive organ benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
female reproductive system disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease female reproductive system disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
female hypogonadism Gene SetFrom HPO Gene-Disease Associations genes associated with the female hypogonadism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
female infertility Gene SetFrom HPO Gene-Disease Associations genes associated with the female infertility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
female pseudohermaphroditism Gene SetFrom HPO Gene-Disease Associations genes associated with the female pseudohermaphroditism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Infertility, Female Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Infertility, Female phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Genital Neoplasms, Female Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genital Neoplasms, Female phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Genital Diseases, Female Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genital Diseases, Female phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Meiosis arrest female protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Meiosis arrest female protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal female reproductive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female meiosis i arrest Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female meiosis i arrest phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
female preputial gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the female preputial gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive system morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
female infertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the female infertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced female fertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced female fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female meiosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female germ cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female germ cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed female fertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed female fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female preputial gland morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female preputial gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female urethra morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive gland morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[analgesia from kappa-opioid receptor agonist, female-specific] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [analgesia from kappa-opioid receptor agonist, female-specific] phenotype from the curated OMIM Gene-Disease Associations dataset. |
luteinizing hormone resistance, female Gene SetFrom OMIM Gene-Disease Associations genes associated with the luteinizing hormone resistance, female phenotype from the curated OMIM Gene-Disease Associations dataset. |
female Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term female in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Female RO_01508 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 Female RO_01508 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 Female RO_01549 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 Female RO_01549 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 Female RO_01480 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 Female RO_01480 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 Female RO_01536 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 Female RO_01536 relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Skeletal Muscle Female Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Skeletal Muscle Female relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
female reproductive gland Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue female reproductive gland from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
female reproductive system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue female reproductive system from the TISSUES Curated Tissue Protein Expression Evidence Scores 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. |
female pudendum Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue female pudendum from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
female reproductive system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue female reproductive system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
female reproductive gland Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue female reproductive gland in proteomics datasets from the TISSUES Experimental 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. |
female reproductive gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue female reproductive gland 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. |
female reproductive system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue female reproductive system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
female cone Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue female cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
female urethra Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue female urethra in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
female pudendum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue female pudendum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Female Breast Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Breast Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Subfertility, Female Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Subfertility, Female in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Hypogonadism Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Hypogonadism Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Female Reproductive System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Female Reproductive System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Female Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Female Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Infertility Associated With Anovulation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Infertility Associated With Anovulation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infiltrating Duct Carcinoma Of Female Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infiltrating Duct Carcinoma Of Female Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
46, Xy Female Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease 46, Xy Female in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Pseudohermaphroditism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Pseudohermaphroditism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Sexual Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Pseudo-Turner Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Pseudo-Turner Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystocele (Female) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystocele (Female) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dyspareunia (Female) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dyspareunia (Female) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Anorgasmia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Anorgasmia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Athlete Triad Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Athlete Triad Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Luteinizing Hormone Resistance, Female Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Luteinizing Hormone Resistance, Female in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Increased Analgesia From Kappa-Opioid Receptor Agonist, Female-Specific (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Increased Analgesia From Kappa-Opioid Receptor Agonist, Female-Specific (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Stress Incontinence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Stress Incontinence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Precocious Female Puberty Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Precocious Female Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Pattern Alopecia (Disorder) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Pattern Alopecia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Breast Pain Female Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Breast Pain Female in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Pelvic Pain Of Female Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Pelvic Pain Of Female in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Female Infertility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Infertility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Female Sterility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Sterility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Female Libido Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Female Libido in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Female Libido Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Female Libido in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pelvic Pain Female Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pelvic Pain Female in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Female Virilization Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Virilization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Female Puberty Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Delayed Female Puberty Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Female Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
female gonad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the female gonad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
female meiosis I Gene SetFrom GO Biological Process Annotations 2023 genes participating in the female meiosis I biological process from the curated GO Biological Process Annotations 2023 dataset. |
female gamete generation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the female gamete generation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of female gonad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
development of primary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2023 genes participating in the development of primary female sexual characteristics biological process from the curated GO Biological Process Annotations 2023 dataset. |
development of secondary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2023 genes participating in the development of secondary female sexual characteristics biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of female gonad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
female pronucleus Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the female pronucleus cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
female germ cell nucleus Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the female germ cell nucleus cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
abnormal female germ cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female germ cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced female fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced female fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
female infertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the female infertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female meiosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female meiosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female reproductive system morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female reproductive system morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased aggression towards female mice Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased aggression towards female mice phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired sperm migration in female genital tract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired sperm migration in female genital tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female reproductive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female reproductive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed female fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed female fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female meiosis I arrest Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female meiosis I arrest phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased female germ cell apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased female germ cell apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female urethra morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female urethra morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent female preputial gland Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent female preputial gland phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
female preputial gland hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the female preputial gland hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enhanced female fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced female fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sperm migration in female genital tract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sperm migration in female genital tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female germ cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female germ cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
female infertility Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the female infertility phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Female steroid hormones in cardiomyocyte energy metabolism Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Female steroid hormones in cardiomyocyte energy metabolism pathway from the WikiPathways Pathways 2024 dataset. |
female meiosis chromosome segregation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female meiosis chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset. |
female gonad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female gonad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
female meiosis I Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female meiosis I biological process from the curated GO Biological Process Annotations 2025 dataset. |
female meiotic nuclear division Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female meiotic nuclear division biological process from the curated GO Biological Process Annotations 2025 dataset. |
female gamete generation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female gamete generation biological process from the curated GO Biological Process Annotations 2025 dataset. |
female pronucleus assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female pronucleus assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of female gonad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
epigenetic programing of female pronucleus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the epigenetic programing of female pronucleus biological process from the curated GO Biological Process Annotations 2025 dataset. |
spindle assembly involved in female meiosis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the spindle assembly involved in female meiosis biological process from the curated GO Biological Process Annotations 2025 dataset. |
development of primary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2025 genes participating in the development of primary female sexual characteristics biological process from the curated GO Biological Process Annotations 2025 dataset. |
development of secondary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2025 genes participating in the development of secondary female sexual characteristics biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of female gonad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
female pronucleus Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the female pronucleus cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
female germ cell nucleus Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the female germ cell nucleus cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Female reproductive system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Female reproductive system disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Female reproductive organ cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Female reproductive organ cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Female reproductive system disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Female reproductive system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive organ cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Female reproductive organ cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive organ benign neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Female reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive organ cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female reproductive organ cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female reproductive system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female breast carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female breast carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive organ benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female breast cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female breast cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive endometrioid cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female reproductive endometrioid cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Prolapse of female genital organ Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Prolapse of female genital organ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female urethral cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female urethral cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female stress incontinence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female stress incontinence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Inhibited female orgasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inhibited female orgasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
female-restricted syndromic X-linked intellectual disability 99 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease female-restricted syndromic X-linked intellectual disability 99 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female infertility of uterine origin Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female infertility of uterine origin in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female breast nipple and areola cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female breast nipple and areola cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive gland Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Female reproductive gland from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Female reproductive system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Female reproductive system from the TISSUES Curated Tissue Protein Expression 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. |
Female pudendum Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Female pudendum from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Female reproductive system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Female reproductive system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Female reproductive gland Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Female reproductive gland in proteomics datasets from the TISSUES Experimental 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. |
Female reproductive gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female reproductive gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female reproductive system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female reproductive system in abstracts of biomedical publications from the TISSUES Text-mining 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. |
Female pudendum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female pudendum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female accessory gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female accessory gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female inflorescence Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female inflorescence in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female urethra Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female urethra in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female cone Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female pronucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Female pronucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Female germ cell nucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Female germ cell nucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Female germ cell nucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Female germ cell nucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Female pronucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Female pronucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Female germline ring canal Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Female germline ring canal cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Female infertility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Female infertility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Female infertility due to zona pellucida defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Female infertility due to zona pellucida defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Facial attractiveness (female raters) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Facial attractiveness (female raters) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Sexual dysfunction (female) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sexual dysfunction (female) 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; 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. |
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. |
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. |
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. |
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. |
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. |
abnormality of the labia minora Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the palmar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary tract abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary tract abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the lymphoid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the lymphoid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized abnormality of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the glial cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the glial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aryepiglottic fold Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aryepiglottic fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the erythroid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prothrombin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prothrombin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the subungual region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the subungual region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thyroid morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thyroid morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the scalp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the retinal pigment epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal collecting system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal collecting system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the middle phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nerves Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |