Name

[skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 2, blond hair/fair skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 2, blond hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 6, blond/brown hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 6, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 10, blond/brown hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 10, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 7, blond/brown hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 7, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 1, blond/brown hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 1, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

Skin/hair/eye pigmentation, variation in, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

[skin/hair/eye pigmentation, variation in, 8] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation, variation in, 8] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 2, red hair/fair skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 2, red hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 9, dark/light hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 9, dark/light hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 5, black/nonblack hair] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 5, black/nonblack hair] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 3, light/dark/freckling skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 3, light/dark/freckling skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 5, dark/fair skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 5, dark/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 4, fair/dark skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 4, fair/dark skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 3, blue/green eyes] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 3, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 6, blue/green eyes] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 6, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 1, blue/nonblue eyes] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 1, blue/nonblue eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 5, dark/light eyes] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 5, dark/light eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 9, brown/nonbrown eyes] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 9, brown/nonbrown eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.

black vs blond hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease black vs blond hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blond vs brown hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blond vs brown hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Blond vs. brown hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blond vs. brown hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Black vs. blond hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Black vs. blond hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

regulation of eye pigmentation Gene Set

From GO Biological Process Annotations

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

negative regulation of eye pigmentation Gene Set

From GO Biological Process Annotations

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

positive regulation of eye pigmentation Gene Set

From GO Biological Process Annotations

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

eye pigmentation Gene Set

From GO Biological Process Annotations

genes participating in the eye pigmentation biological process from the curated GO Biological Process Annotations dataset.

absent eye pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal eye pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

decreased eye pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blond Gene Set

From GeneRIF Biological Term Annotations

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

eye infections, fungal; fungal eye infections; histoplasmosis; neovascularization, pathologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye infections, fungal; fungal eye infections; histoplasmosis; neovascularization, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye neoplasms; melanoma; tumour of eye Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye neoplasms; melanoma; tumour of eye in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormality of hair pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of hair pigmentation Gene Set

From HPO Gene-Disease Associations

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

abnormal hind foot hair pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal coat/hair pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal tail hair pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pinna hair pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

Skin Pigmentation Gene Set

From dbGAP Gene-Trait Associations

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

skin pigmentation Gene Set

From GAD Gene-Disease Associations

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

Skin pigmentation Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Skin pigmentation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormality of skin pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

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

reticulated skin pigmentation Gene Set

From HPO Gene-Disease Associations

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

fine, reticulate skin pigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the fine, reticulate skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

blotching pigmentation of the skin Gene Set

From HPO Gene-Disease Associations

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

pigmentation anomalies of sun-exposed skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of skin pigmentation Gene Set

From HPO Gene-Disease Associations

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

absent skin pigmentation Gene Set

From HPO Gene-Disease Associations

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

decreased skin pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal skin pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

absent skin pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

eye diseases; sarcoidosis; skin diseases Gene Set

From GAD Gene-Disease Associations

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

colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Impdh2 enzyme activity, variation in Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Impdh2 enzyme activity, variation in phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Apocrine gland secretion, variation in Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Apocrine gland secretion, variation in phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

QT INTERVAL, VARIATION IN Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease QT INTERVAL, VARIATION IN from the curated CTD Gene-Disease Associations dataset.

quantitative variation in lipid and lipoprotein traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease quantitative variation in lipid and lipoprotein traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

normmal variation Gene Set

From GAD Gene-Disease Associations

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

normal variation in leptin levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease normal variation in leptin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nomal variation Gene Set

From GAD Gene-Disease Associations

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

pharmacogenetic variation Gene Set

From GAD Gene-Disease Associations

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

dyslexia; reading; normal variation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyslexia; reading; normal variation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

variation in platelet integrin alpha 2 beta 1 density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease variation in platelet integrin alpha 2 beta 1 density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

variation in plasma lipoproteins Gene Set

From GAD Gene-Disease Associations

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

quantitative variation in plasma high-density lipoproteins and triacylglycerides Gene Set

From GAD Gene-Disease Associations

genes associated with the disease quantitative variation in plasma high-density lipoproteins and triacylglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

normal variation Gene Set

From GAD Gene-Disease Associations

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

variation Gene Set

From GeneRIF Biological Term Annotations

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

DNA methylation (variation) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the DNA methylation (variation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

patchy variation in bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy variation in bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

[axillary odor, variation in] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [axillary odor, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.

[colostrum secretion, variation in] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [colostrum secretion, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.

[qt interval, variation in] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [qt interval, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.

{gene expression, variation in, qtl} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {gene expression, variation in, qtl} phenotype from the curated OMIM Gene-Disease Associations dataset.

[impdh2 enzyme activity, variation in] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [impdh2 enzyme activity, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density variation qtl] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density variation qtl] phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, variation in} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, variation in} phenotype from the curated OMIM Gene-Disease Associations dataset.

[hair morphology 1, hair thickness] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [hair morphology 1, hair thickness] phenotype from the curated OMIM Gene-Disease Associations dataset.

Skin fragility woolly hair syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin fragility woolly hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin Fragility-Woolly Hair Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skin Fragility-Woolly Hair Syndrome from the curated CTD Gene-Disease Associations dataset.

cutaneous melanoma which is largely independent of skin type and hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cutaneous melanoma which is largely independent of skin type and hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin fragility-woolly hair syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the skin fragility-woolly hair syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; melanoma; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; melanoma; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanocyte development and pigmentation pathway Gene Set

From Biocarta Pathways

proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.

Pigmentation Disorders Gene Set

From CTD Gene-Disease Associations

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

Epidermolysis bullosa simplex with mottled pigmentation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis bullosa simplex with mottled pigmentation from the curated CTD Gene-Disease Associations dataset.

pigmentation disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

pigmentation disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

conjunctival pigmentation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

human pigmentation Gene Set

From GAD Gene-Disease Associations

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

pigmentation Gene Set

From GAD Gene-Disease Associations

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

exfoliation syndrome; glaucoma, open-angle; pigmentation disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exfoliation syndrome; glaucoma, open-angle; pigmentation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; pigmentation Gene Set

From GAD Gene-Disease Associations

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

hemochromatosis; iron overload; pigmentation disorders Gene Set

From GAD Gene-Disease Associations

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

pigmentation Gene Set

From GeneRIF Biological Term Annotations

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

pigmentation Gene Set

From GO Biological Process Annotations

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

cellular pigmentation Gene Set

From GO Biological Process Annotations

genes participating in the cellular pigmentation biological process from the curated GO Biological Process Annotations dataset.

regulation of developmental pigmentation Gene Set

From GO Biological Process Annotations

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

negative regulation of developmental pigmentation Gene Set

From GO Biological Process Annotations

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

pigment metabolic process involved in pigmentation Gene Set

From GO Biological Process Annotations

genes participating in the pigment metabolic process involved in pigmentation biological process from the curated GO Biological Process Annotations dataset.

pigment metabolic process involved in developmental pigmentation Gene Set

From GO Biological Process Annotations

genes participating in the pigment metabolic process involved in developmental pigmentation biological process from the curated GO Biological Process Annotations dataset.

developmental pigmentation Gene Set

From GO Biological Process Annotations

genes participating in the developmental pigmentation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of developmental pigmentation Gene Set

From GO Biological Process Annotations

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

abnormal iris pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

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

absent pigmentation of chest Gene Set

From HPO Gene-Disease Associations

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

rarefaction of retinal pigmentation Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal pigmentation abnormalities Gene Set

From HPO Gene-Disease Associations

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

abnormal pigmentation of the oral mucosa Gene Set

From HPO Gene-Disease Associations

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

pigmentation of the sclera Gene Set

From HPO Gene-Disease Associations

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

decreased retinal pigmentation with dispersion Gene Set

From HPO Gene-Disease Associations

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

mottled pigmentation Gene Set

From HPO Gene-Disease Associations

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

mottled pigmentation of the trunk and proximal extremities Gene Set

From HPO Gene-Disease Associations

genes associated with the mottled pigmentation of the trunk and proximal extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal retinal pigmentation Gene Set

From HPO Gene-Disease Associations

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

absent pigmentation of the ventral chest Gene Set

From HPO Gene-Disease Associations

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

abnormality of macular pigmentation Gene Set

From HPO Gene-Disease Associations

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

abnormal iris pigmentation Gene Set

From HPO Gene-Disease Associations

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

atypical nevi (>5mm with irregular edge and pigmentation) Gene Set

From HPO Gene-Disease Associations

genes associated with the atypical nevi (>5mm with irregular edge and pigmentation) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Pigmentation Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

increased ear pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ear pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal otic pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal extracutaneous pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal foot pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal epidermal pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal digit pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal agouti pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal dermal pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal iris pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ventral coat pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal tail pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

irregular coat pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ciliary body pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

decreased ear pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal choroid pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

pigmentation phenotype Gene Set

From MPO Gene-Phenotype Associations

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

increased tail pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal harderian gland pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

absent coat pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal iris stromal pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

decreased tail pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

decreased foot pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscle eye brain disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscle eye brain disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fish-eye disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fish-eye disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Eye Diseases, Hereditary Gene Set

From CTD Gene-Disease Associations

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

Eye Abnormalities Gene Set

From CTD Gene-Disease Associations

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

Eye Diseases Gene Set

From CTD Gene-Disease Associations

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

Aland Island Eye Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aland Island Eye Disease from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma from the curated CTD Gene-Disease Associations dataset.

Dry Eye Syndromes Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dry Eye Syndromes from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

Eye Pain Gene Set

From CTD Gene-Disease Associations

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

Eye Infections, Bacterial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Eye Infections, Bacterial from the curated CTD Gene-Disease Associations dataset.

Eye Gene Set

From dbGAP Gene-Trait Associations

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

Eye Color Gene Set

From dbGAP Gene-Trait Associations

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

eye disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

eye and adnexa disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

eye disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

eye and adnexa disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

eye disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eye degenerative disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eye lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eye carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

shipyard eye Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dry eye syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

aland island eye disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eye accommodation disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eye and adnexa disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eye color Gene Set

From GAD Gene-Disease Associations

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

eye diseases; retinal diseases Gene Set

From GAD Gene-Disease Associations

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

eye diseases; hypersensitivity; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases; hypersensitivity; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye abnormalities Gene Set

From GAD Gene-Disease Associations

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

eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anophthalmos; coloboma; eye abnormalities; microphthalmos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anophthalmos; coloboma; eye abnormalities; microphthalmos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; eye diseases; hyperhomocysteinemia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; eye diseases; hyperhomocysteinemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aphakia; eye abnormalities; microphthalmos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aphakia; eye abnormalities; microphthalmos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases Gene Set

From GAD Gene-Disease Associations

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

eye movement disturbances Gene Set

From GAD Gene-Disease Associations

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

dry eye syndromes; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dry eye syndromes; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; corneal diseases; dry eye syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; corneal diseases; dry eye syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye Gene Set

From GAD Gene-Disease Associations

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

eye diseases, hereditary; pseudoxanthoma elasticum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; pseudoxanthoma elasticum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye abnormalities; glaucoma, angle-closure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye abnormalities; glaucoma, angle-closure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fish eye disease Gene Set

From GAD Gene-Disease Associations

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

eye diseases; glomerulosclerosis, focal segmental; nephrotic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases; glomerulosclerosis, focal segmental; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; eye diseases; Gene Set

From GAD Gene-Disease Associations

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

eye diseases; stevens-johnson syndrome Gene Set

From GAD Gene-Disease Associations

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

corneal ulcer; eye infections, bacterial; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease corneal ulcer; eye infections, bacterial; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

smooth pursuit eye movement abnormality Gene Set

From GAD Gene-Disease Associations

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

eye Gene Set

From GeneRIF Biological Term Annotations

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

embryonic eye morphogenesis Gene Set

From GO Biological Process Annotations

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

eye photoreceptor cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the eye photoreceptor cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

retina development in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the retina development in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

eye pigment granule organization Gene Set

From GO Biological Process Annotations

genes participating in the eye pigment granule organization biological process from the curated GO Biological Process Annotations dataset.

post-embryonic eye morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the post-embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations dataset.

eye photoreceptor cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations dataset.

eye morphogenesis Gene Set

From GO Biological Process Annotations

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

post-embryonic retina morphogenesis in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the post-embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

eyelid development in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the eyelid development in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

camera-type eye photoreceptor cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the camera-type eye photoreceptor cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

optic cup morphogenesis involved in camera-type eye development Gene Set

From GO Biological Process Annotations

genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations dataset.

embryonic camera-type eye morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the embryonic camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations dataset.

compound eye corneal lens development Gene Set

From GO Biological Process Annotations

genes participating in the compound eye corneal lens development biological process from the curated GO Biological Process Annotations dataset.

cornea development in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the cornea development in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

eye pigment metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the eye pigment metabolic process biological process from the curated GO Biological Process Annotations dataset.

camera-type eye development Gene Set

From GO Biological Process Annotations

genes participating in the camera-type eye development biological process from the curated GO Biological Process Annotations dataset.

embryonic retina morphogenesis in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

camera-type eye morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations dataset.

eye pigment biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the eye pigment biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

embryonic camera-type eye development Gene Set

From GO Biological Process Annotations

genes participating in the embryonic camera-type eye development biological process from the curated GO Biological Process Annotations dataset.

retina vasculature development in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

camera-type eye photoreceptor cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the camera-type eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations dataset.

retina morphogenesis in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

lens development in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the lens development in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

embryonic camera-type eye formation Gene Set

From GO Biological Process Annotations

genes participating in the embryonic camera-type eye formation biological process from the curated GO Biological Process Annotations dataset.

regulation of retina development in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retina development in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

eye development Gene Set

From GO Biological Process Annotations

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

retina vasculature morphogenesis in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the retina vasculature morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

lens morphogenesis in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the lens morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

optic cup formation involved in camera-type eye development Gene Set

From GO Biological Process Annotations

genes participating in the optic cup formation involved in camera-type eye development biological process from the curated GO Biological Process Annotations dataset.

eye photoreceptor cell development Gene Set

From GO Biological Process Annotations

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

optic placode formation involved in camera-type eye formation Gene Set

From GO Biological Process Annotations

genes participating in the optic placode formation involved in camera-type eye formation biological process from the curated GO Biological Process Annotations dataset.

post-embryonic camera-type eye morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the post-embryonic camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations dataset.

compound eye development Gene Set

From GO Biological Process Annotations

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

lens induction in camera-type eye Gene Set

From GO Biological Process Annotations

genes participating in the lens induction in camera-type eye biological process from the curated GO Biological Process Annotations dataset.

post-embryonic camera-type eye development Gene Set

From GO Biological Process Annotations

genes participating in the post-embryonic camera-type eye development biological process from the curated GO Biological Process Annotations dataset.

structural constituent of eye lens Gene Set

From GO Molecular Function Annotations

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

Eye color traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Eye color traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Eye color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Eye color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

eye disease Gene Set

From GWASdb SNP-Disease Associations

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

eye and adnexa disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormal eye physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the posterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of eye movement Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the anterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal eye morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the vasculature of the eye Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the eye Gene Set

From GWASdb SNP-Phenotype Associations

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

aplasia/hypoplasia affecting the eye Gene Set

From HPO Gene-Disease Associations

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

neoplasm of the eye Gene Set

From HPO Gene-Disease Associations

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

abnormality of the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

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

abnormality of saccadic eye movements Gene Set

From HPO Gene-Disease Associations

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

slow saccadic eye movements Gene Set

From HPO Gene-Disease Associations

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

deeply set eye Gene Set

From HPO Gene-Disease Associations

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

abnormality of the eye Gene Set

From HPO Gene-Disease Associations

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

inflammatory abnormality of the eye Gene Set

From HPO Gene-Disease Associations

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

eye of the tiger anomaly of globus pallidus Gene Set

From HPO Gene-Disease Associations

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

bull's eye maculopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the bull's eye maculopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal eye physiology Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia affecting the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

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

hemorrhage of the eye Gene Set

From HPO Gene-Disease Associations

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

uncontrolled eye movements Gene Set

From HPO Gene-Disease Associations

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

poor hand-eye coordination Gene Set

From HPO Gene-Disease Associations

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

anterior segment of eye aplasia Gene Set

From HPO Gene-Disease Associations

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

abnormal conjugate eye movement Gene Set

From HPO Gene-Disease Associations

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

hamartoma of the eye Gene Set

From HPO Gene-Disease Associations

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

paroxysmal involuntary eye movements Gene Set

From HPO Gene-Disease Associations

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

eye poking Gene Set

From HPO Gene-Disease Associations

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

abnormal eye morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the vasculature of the eye Gene Set

From HPO Gene-Disease Associations

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

poor eye contact Gene Set

From HPO Gene-Disease Associations

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

abnormal rapid eye movement (rem) sleep Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the posterior segment of the eye Gene Set

From HPO Gene-Disease Associations

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

abnormality of eye movement Gene Set

From HPO Gene-Disease Associations

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

abnormal involuntary eye movements Gene Set

From HPO Gene-Disease Associations

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

absent anterior eye chamber Gene Set

From HPO Gene-Disease Associations

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

Eye Hemorrhage Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Eye Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Eye Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Eye Infections, Fungal Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Eye Infections, Fungal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Eye Infections, Viral Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Eye Infections, Viral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Eye Infections, Bacterial Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Eye Infections, Bacterial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cat eye syndrome critical region protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cat eye syndrome critical region protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cat eye syndrome critical region protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cat eye syndrome critical region protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cat eye syndrome critical region protein 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cat eye syndrome critical region protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal eye morphology Gene Set

From MPO Gene-Phenotype Associations

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

hydropic eye lens fibers Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hydropic eye lens fibers phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal non-rapid eye movement sleep pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

eye hemorrhage Gene Set

From MPO Gene-Phenotype Associations

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

abnormal eye posterior chamber morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal eye posterior chamber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal eye pigment epithelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal eye pigment epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal eye electrophysiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal eye distance/ position Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal eye distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

eye opacity Gene Set

From MPO Gene-Phenotype Associations

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

vision/eye phenotype Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vision/eye phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal eye anterior chamber morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal eye anterior chamber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged eye anterior chamber Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged eye anterior chamber phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

eye bleb Gene Set

From MPO Gene-Phenotype Associations

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

abnormal eye muscle morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal eye muscle development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal eye muscle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal eye anterior chamber depth Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal eye anterior chamber depth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal eye physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal eye development Gene Set

From MPO Gene-Phenotype Associations

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

narrow eye opening Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the narrow eye opening phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal eye movement Gene Set

From MPO Gene-Phenotype Associations

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

abnormal anterior eye segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal eye size Gene Set

From MPO Gene-Phenotype Associations

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

abnormal posterior eye segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal posterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal eye blink conditioning behavior Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal eye blink conditioning behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

eye inflammation Gene Set

From MPO Gene-Phenotype Associations

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

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

fish-eye disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the fish-eye disease phenotype from the curated OMIM Gene-Disease Associations dataset.

microtia with nasolacrimal duct imperforation and eye coloboma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microtia with nasolacrimal duct imperforation and eye coloboma phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

cat eye syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cat eye syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

aland island eye disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the aland island eye disease phenotype from the curated OMIM Gene-Disease Associations dataset.

bornholm eye disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the bornholm eye disease phenotype from the curated OMIM Gene-Disease Associations dataset.

eye Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

eye cancer cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

eye Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

anterior chamber of the eye Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

vitreous chamber of the eye Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

posterior chamber of the eye Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

compound eye Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

eye cancer cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

chamber of the eye Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

eye Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Woolly hair, autosomal recessive 2, with or without hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Woolly hair, autosomal recessive 2, with or without hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy dilated with woolly hair and keratoderma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Menkes kinky-hair syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Menkes kinky-hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

root hair tip Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

cell hair Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

root hair Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

Hair Dyes Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Hair Dyes from the curated CTD Gene-Chemical Interactions dataset.

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

From CTD Gene-Disease Associations

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

WOOLLY HAIR, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease WOOLLY HAIR, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Menkes Kinky Hair Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Menkes Kinky Hair Syndrome from the curated CTD Gene-Disease Associations dataset.

Hair Diseases Gene Set

From CTD Gene-Disease Associations

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

Cartilage-hair hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cartilage-hair hypoplasia from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy dilated with Woolly hair and keratoderma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair and keratoderma from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR from the curated CTD Gene-Disease Associations dataset.

ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE from the curated CTD Gene-Disease Associations dataset.

Woolly hair, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Woolly hair, congenital from the curated CTD Gene-Disease Associations dataset.

Hair Gene Set

From dbGAP Gene-Trait Associations

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

Hair Color Gene Set

From dbGAP Gene-Trait Associations

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

hair disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hair follicle neoplasm Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hair disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

hair follicle neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cartilage-hair hypoplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hair disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

black vs red hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease black vs red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hair color Gene Set

From GAD Gene-Disease Associations

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

ultrastructure of the hair Gene Set

From GAD Gene-Disease Associations

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

hair thickness Gene Set

From GAD Gene-Disease Associations

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

red vs non-red hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease red vs non-red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

straight hair Gene Set

From GAD Gene-Disease Associations

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

hair morphology Gene Set

From GAD Gene-Disease Associations

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

hair Gene Set

From GAD Gene-Disease Associations

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

hair colour Gene Set

From GAD Gene-Disease Associations

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

hair Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of hair follicle maturation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations dataset.

hair follicle placode formation Gene Set

From GO Biological Process Annotations

genes participating in the hair follicle placode formation biological process from the curated GO Biological Process Annotations dataset.

hair follicle development Gene Set

From GO Biological Process Annotations

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

negative regulation of root hair elongation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of root hair elongation biological process from the curated GO Biological Process Annotations dataset.

regulation of root hair elongation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of root hair elongation biological process from the curated GO Biological Process Annotations dataset.

regulation of hair cycle by canonical wnt signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hair cycle by canonical wnt signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hair cycle Gene Set

From GO Biological Process Annotations

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

regulation of hair follicle maturation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations dataset.

hair cycle phase Gene Set

From GO Biological Process Annotations

genes participating in the hair cycle phase biological process from the curated GO Biological Process Annotations dataset.

hair cell differentiation Gene Set

From GO Biological Process Annotations

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

regulation of hair follicle development Gene Set

From GO Biological Process Annotations

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

establishment of body hair planar orientation Gene Set

From GO Biological Process Annotations

genes participating in the establishment of body hair planar orientation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of hair follicle cell proliferation Gene Set

From GO Biological Process Annotations

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

hair cycle process Gene Set

From GO Biological Process Annotations

genes participating in the hair cycle process biological process from the curated GO Biological Process Annotations dataset.

regulation of hair follicle cell proliferation Gene Set

From GO Biological Process Annotations

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

positive regulation of hair cycle Gene Set

From GO Biological Process Annotations

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

regulation of hair cycle Gene Set

From GO Biological Process Annotations

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

negative regulation of hair follicle development Gene Set

From GO Biological Process Annotations

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

positive regulation of hair follicle development Gene Set

From GO Biological Process Annotations

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

positive regulation of hair follicle maturation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations dataset.

establishment of body hair or bristle planar orientation Gene Set

From GO Biological Process Annotations

genes participating in the establishment of body hair or bristle planar orientation biological process from the curated GO Biological Process Annotations dataset.

hair follicle morphogenesis Gene Set

From GO Biological Process Annotations

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

hair cycle Gene Set

From GO Biological Process Annotations

genes participating in the hair cycle biological process from the curated GO Biological Process Annotations dataset.

hair follicle cell proliferation Gene Set

From GO Biological Process Annotations

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

hair follicle maturation Gene Set

From GO Biological Process Annotations

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

Red vs non-red hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Red vs non-red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hair morphology Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hair morphology phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Black vs. red hair color Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Black vs. red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

hair disease Gene Set

From GWASdb SNP-Disease Associations

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

red hair Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal hair quantity Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the hair Gene Set

From GWASdb SNP-Phenotype Associations

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

acquired abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

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

patchy hypopigmentation of hair Gene Set

From HPO Gene-Disease Associations

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

brittle hair Gene Set

From HPO Gene-Disease Associations

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

abnormality of secondary sexual hair Gene Set

From HPO Gene-Disease Associations

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

sparse body hair Gene Set

From HPO Gene-Disease Associations

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

hypopigmentation of hair Gene Set

From HPO Gene-Disease Associations

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

red hair Gene Set

From HPO Gene-Disease Associations

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

frontal upsweep of hair Gene Set

From HPO Gene-Disease Associations

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

fair hair Gene Set

From HPO Gene-Disease Associations

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

congenital abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

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

absent facial hair Gene Set

From HPO Gene-Disease Associations

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

projection of scalp hair onto lateral cheek Gene Set

From HPO Gene-Disease Associations

genes associated with the projection of scalp hair onto lateral cheek phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sparse scalp hair Gene Set

From HPO Gene-Disease Associations

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

premature graying of hair Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pubic hair Gene Set

From HPO Gene-Disease Associations

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

slow-growing hair Gene Set

From HPO Gene-Disease Associations

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

absent pubic hair Gene Set

From HPO Gene-Disease Associations

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

generalized hypopigmentation of hair Gene Set

From HPO Gene-Disease Associations

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

abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

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

abnormality of hair growth rate Gene Set

From HPO Gene-Disease Associations

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

sparse hair Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hair Gene Set

From HPO Gene-Disease Associations

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

curly hair Gene Set

From HPO Gene-Disease Associations

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

melanin pigment aggregation in hair shafts Gene Set

From HPO Gene-Disease Associations

genes associated with the melanin pigment aggregation in hair shafts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

coarse hair Gene Set

From HPO Gene-Disease Associations

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

abnormality of hair texture Gene Set

From HPO Gene-Disease Associations

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

scalp hair loss Gene Set

From HPO Gene-Disease Associations

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

absent axillary hair Gene Set

From HPO Gene-Disease Associations

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

abnormality of the scalp hair Gene Set

From HPO Gene-Disease Associations

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

thick hair Gene Set

From HPO Gene-Disease Associations

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

woolly hair Gene Set

From HPO Gene-Disease Associations

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

dry hair Gene Set

From HPO Gene-Disease Associations

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

sparse facial hair Gene Set

From HPO Gene-Disease Associations

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

abnormal hair quantity Gene Set

From HPO Gene-Disease Associations

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

extension of hair growth on temples to lateral eyebrow Gene Set

From HPO Gene-Disease Associations

genes associated with the extension of hair growth on temples to lateral eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

silver-gray hair Gene Set

From HPO Gene-Disease Associations

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

abnormal hair laboratory examination Gene Set

From HPO Gene-Disease Associations

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

abnormal hair whorl Gene Set

From HPO Gene-Disease Associations

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

fine hair Gene Set

From HPO Gene-Disease Associations

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

sparse pubic hair Gene Set

From HPO Gene-Disease Associations

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

large clumps of pigment irregularly distributed along hair shaft Gene Set

From HPO Gene-Disease Associations

genes associated with the large clumps of pigment irregularly distributed along hair shaft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hair-nail ectodermal dysplasia Gene Set

From HPO Gene-Disease Associations

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

abnormality of the axillary hair Gene Set

From HPO Gene-Disease Associations

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

abnormality of hair density Gene Set

From HPO Gene-Disease Associations

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

acquired abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

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

white hair Gene Set

From HPO Gene-Disease Associations

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

hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes Gene Set

From HPO Gene-Disease Associations

genes associated with the hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent hair Gene Set

From HPO Gene-Disease Associations

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

sparse axillary hair Gene Set

From HPO Gene-Disease Associations

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

vestibular hair cell degeneration Gene Set

From MPO Gene-Phenotype Associations

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

retarded hair growth Gene Set

From MPO Gene-Phenotype Associations

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

whorled hair Gene Set

From MPO Gene-Phenotype Associations

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

long hair Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair shaft morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal outer hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal outer hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cochlear hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

brittle hair Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair medulla air spaces Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair medulla air spaces phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal zigzag hair morphology Gene Set

From MPO Gene-Phenotype Associations

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

cochlear inner hair cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cochlear inner hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair follicle pheomelanosome pheomelanin Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle pheomelanosome pheomelanin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal auchene hair morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent hair follicle inner root sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle inner root sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cochlear hair cell degeneration Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair cycle telogen phase Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cycle telogen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cochlear hair bundle ankle links Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear hair bundle ankle links phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear inner hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

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

thin vestibular hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin vestibular hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair follicle melanin granules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle melanin granules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair bundle inter-stereocilial links Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair bundle inter-stereocilial links phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin hair shaft Gene Set

From MPO Gene-Phenotype Associations

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

abnormal orientation of inner hair cell stereociliary bundles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal orientation of inner hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair-down neuron morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair-down neuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cuticle Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair follicle dermal papilla morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle dermal papilla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair follicle dermal papilla Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle dermal papilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent guard hair Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inner hair cell kinocilium morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased vestibular hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vestibular hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vestibular hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cochlear hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated hair follicles Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair follicle infundibulum morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle infundibulum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

underdeveloped hair follicles Gene Set

From MPO Gene-Phenotype Associations

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

distended hair follicles Gene Set

From MPO Gene-Phenotype Associations

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

decreased zigzag hair amount Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair follicle outer root sheath morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle outer root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal outer hair cell kinocilium morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased hair follicle apoptosis Gene Set

From MPO Gene-Phenotype Associations

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

hair follicle degeneration Gene Set

From MPO Gene-Phenotype Associations

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

abnormal awl hair morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased hair follicle number Gene Set

From MPO Gene-Phenotype Associations

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

absent cochlear outer hair cell electromotility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal orientation of outer hair cell stereociliary bundles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal orientation of outer hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vestibular hair cells Gene Set

From MPO Gene-Phenotype Associations

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

absent hair-down neurons Gene Set

From MPO Gene-Phenotype Associations

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

absent cochlear outer hair cells Gene Set

From MPO Gene-Phenotype Associations

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

sparse hair Gene Set

From MPO Gene-Phenotype Associations

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

thick hair follicle outer rooth sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thick hair follicle outer rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle melanin granule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair shaft melanin granule distribution Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair shaft melanin granule distribution phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short hair Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair growth Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vestibular hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle matrix region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle matrix region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inner hair cell synaptic ribbon morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner hair cell synaptic ribbon morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

coarse hair Gene Set

From MPO Gene-Phenotype Associations

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

absent inner hair cell kinocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner hair cell kinocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair follicle morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal duvet hair morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair cortex keratinization Gene Set

From MPO Gene-Phenotype Associations

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

absent awl hair Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair follicle bulge morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle bulge morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair bundle ankle links morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair bundle ankle links morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle melanogenesis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear outer hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

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

premature hair loss Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear hair bundle tip links morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair bundle tip links morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair shaft melanin granule shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair shaft melanin granule shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cycle anagen phase Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cycle anagen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent cochlear inner hair cells Gene Set

From MPO Gene-Phenotype Associations

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

fused outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fused outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hair follicle outer rooth sheath hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hair follicle outer rooth sheath hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hair follicles Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair medulla Gene Set

From MPO Gene-Phenotype Associations

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

short cochlear hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear outer hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair texture Gene Set

From MPO Gene-Phenotype Associations

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

decreased cochlear outer hair cell electromotility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin cochlear hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

waved hair Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear inner hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal coat/ hair morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal coat/ hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

focal dorsal hair loss Gene Set

From MPO Gene-Phenotype Associations

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

fused inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fused inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased outer hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased outer hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal guard hair morphology Gene Set

From MPO Gene-Phenotype Associations

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

thin hair follicle outer rooth sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin hair follicle outer rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased inner hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased inner hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair cell kinocilium morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent vestibular hair bundle shaft connectors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vestibular hair bundle shaft connectors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair cell inter-stereocilial links morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell inter-stereocilial links morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle orientation Gene Set

From MPO Gene-Phenotype Associations

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

thin hair follicle inner rooth sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin hair follicle inner rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle melanin granule distribution Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle melanin granule distribution phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ruffled hair Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear outer hair cell electromotility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair cell mechanoelectric transduction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cell mechanoelectric transduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

focal hair loss Gene Set

From MPO Gene-Phenotype Associations

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

reduced hair shaft melanin granule number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the reduced hair shaft melanin granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair bundle shaft connectors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair bundle shaft connectors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle pheomelanosome pheomelanin content Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle pheomelanosome pheomelanin content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cycle Gene Set

From MPO Gene-Phenotype Associations

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

absent cochlear hair cells Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair follicle melanocyte morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair shaft melanin granule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair shaft melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased guard hair length Gene Set

From MPO Gene-Phenotype Associations

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

absent active-zone-anchored inner hair cell synaptic ribbon Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent active-zone-anchored inner hair cell synaptic ribbon phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair medullary septa cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair medullary septa cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

progressive hair loss Gene Set

From MPO Gene-Phenotype Associations

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

delayed hair regrowth Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cochlear hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged hair follicles Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair follicle physiology Gene Set

From MPO Gene-Phenotype Associations

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

fused vestibular hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fused vestibular hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cycle catagen phase Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair cycle catagen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small hair follicles Gene Set

From MPO Gene-Phenotype Associations

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

abnormal guard hair length Gene Set

From MPO Gene-Phenotype Associations

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

decreased cochlear outer hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short cochlear outer hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent duvet hair Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vestibular hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle regression Gene Set

From MPO Gene-Phenotype Associations

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

enlarged hair follicle melanin granules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged hair follicle melanin granules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair cortex morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased guard hair length Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear hair cell development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular hair cell development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vestibular hair cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal orientation of cochlear hair cell stereociliary bundles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal orientation of cochlear hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cochlear outer hair cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cochlear outer hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated hair follicle infundibulum Gene Set

From MPO Gene-Phenotype Associations

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

decreased vestibular hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle inner root sheath morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle inner root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased vestibular hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased vestibular hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

distorted hair follicle pattern Gene Set

From MPO Gene-Phenotype Associations

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

accelerated hair follicle regression Gene Set

From MPO Gene-Phenotype Associations

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

delayed hair appearance Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair shedding Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair follicle bulb morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle bulb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

noonan-like syndrome with loose anagen hair Gene Set

From OMIM Gene-Disease Associations

genes associated with the noonan-like syndrome with loose anagen hair phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 6, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 6, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

hair, curly Gene Set

From OMIM Gene-Disease Associations

genes associated with the hair, curly phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, with woolly hair and keratoderma Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, with woolly hair and keratoderma phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 7, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 7, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 5, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 5, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 4, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 4, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

palmoplantar keratoderma and woolly hair Gene Set

From OMIM Gene-Disease Associations

genes associated with the palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal recessive 1, with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal recessive 1, with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 9, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 9, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 8, hair/tooth/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 8, hair/tooth/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal recessive 2 with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal recessive 2 with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.

cartilage-hair hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cartilage-hair hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

hair root Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

hair follicle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

hair Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

hair cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

inner hair cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hair follicle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hair follicle outer root sheath Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair follicle outer root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair shaft Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hair follicle inner root sheath Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair follicle inner root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair follicle bulge Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hair medulla Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

outer hair cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hair root Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

hair follicle bulge stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair follicle bulge stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Hair Follicle Development: Induction (Part 1 of 3)(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Hair Follicle Development: Induction (Part 1 of 3)(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Skin Gene Set

From BioGPS Human Cell Type and Tissue Gene Expression Profiles

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

Inflammatory skin and bowel disease, neonatal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stiff skin syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stiff skin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dominant dystrophic epidermolysis bullosa with absence of skin Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dominant dystrophic epidermolysis bullosa with absence of skin phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypotrichosis and recurrent skin vesicles Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia skin fragility syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia skin fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peeling skin syndrome, acral type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peeling skin syndrome, acral type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tight skin contracture syndrome, lethal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tight skin contracture syndrome, lethal from the curated CTD Gene-Disease Associations dataset.

Skin Diseases Gene Set

From CTD Gene-Disease Associations

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

Skin Abnormalities Gene Set

From CTD Gene-Disease Associations

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

Wrinkly skin syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Wrinkly skin syndrome from the curated CTD Gene-Disease Associations dataset.

Hypotrichosis And Recurrent Skin Vesicles Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.

Skin Diseases, Vascular Gene Set

From CTD Gene-Disease Associations

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

Skin Ulcer Gene Set

From CTD Gene-Disease Associations

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

PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset.

Ectodermal dysplasia/ skin fragility syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia/ skin fragility syndrome from the curated CTD Gene-Disease Associations dataset.

Peeling Skin Syndrome Gene Set

From CTD Gene-Disease Associations

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

Stiff Skin Syndrome Gene Set

From CTD Gene-Disease Associations

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

Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.

Skin Neoplasms Gene Set

From CTD Gene-Disease Associations

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

Peeling skin syndrome, acral type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peeling skin syndrome, acral type from the curated CTD Gene-Disease Associations dataset.

skin disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

vascular skin disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

skin benign neoplasm Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

vesiculobullous skin disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

skin cancer Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

skin disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

vascular skin disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

skin melanoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

verruciform xanthoma of skin Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin squamous cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin sarcoidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

malignant skin fibrous histiocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sarcomatoid squamous cell skin carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autoimmune disease of skin and connective tissue Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autoimmune disease of skin and connective tissue in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bullous skin disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin lipoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin carcinoma in situ Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vesiculobullous skin disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eccrine mixed tumor of skin Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin papilloma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin pilomatrix carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vascular skin disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin sarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin tag Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

chronic ulcer of skin Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin hemangioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin benign neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

H3K4me3_fibroblast of skin of abdomen_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_fibroblast of skin of abdomen_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_fibroblast of skin of abdomen_hg19_2 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_fibroblast of skin of abdomen_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

CTCF_fibroblast of skin of abdomen_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_fibroblast of skin of abdomen_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_fibroblast of skin of abdomen_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_fibroblast of skin of abdomen_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin cancer, nonmelanoma Gene Set

From GAD Gene-Disease Associations

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

melanoma; nevus; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; nevus; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasms, multiple primary; nevus; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, multiple primary; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

behcet syndrome; disease susceptibility; skin diseases Gene Set

From GAD Gene-Disease Associations

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

breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; nevus; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

erythema; psoriasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma, amelanotic; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma, amelanotic; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, t-cell, cutaneous; parapsoriasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, t-cell, cutaneous; parapsoriasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin color Gene Set

From GAD Gene-Disease Associations

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

lung cancer; skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung cancer; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin cancer Gene Set

From GAD Gene-Disease Associations

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

dna damage; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

melanoma; skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin cancer; squamous cell carcinoma; carcinoma, basal cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skin cancer; squamous cell carcinoma; carcinoma, basal cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

psoriasis; skin diseases, genetic Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

papillomavirus infections; skin neoplasms; sunburn; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease papillomavirus infections; skin neoplasms; sunburn; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasm invasiveness; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

erythema; rare diseases; skin diseases Gene Set

From GAD Gene-Disease Associations

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

skin condition Gene Set

From GAD Gene-Disease Associations

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

neoplasms, basal cell; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, basal cell; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; skin basal cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; skin basal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin diseases; sunburn Gene Set

From GAD Gene-Disease Associations

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

dna damage; neoplasms; skin diseases Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

carcinoma, basal cell; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; melanoma; neoplasm metastasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; melanoma; neoplasm metastasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin carcinomas Gene Set

From GAD Gene-Disease Associations

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

cell transformation, neoplastic; epidermodysplasia verruciformis; papillomavirus infections; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cell transformation, neoplastic; epidermodysplasia verruciformis; papillomavirus infections; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cell transformation, neoplastic; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cell transformation, neoplastic; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lupus erythematosus, cutaneous; lupus erythematosus, discoid; photosensitivity disorders; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus, cutaneous; lupus erythematosus, discoid; photosensitivity disorders; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

edema; hypertension; skin diseases Gene Set

From GAD Gene-Disease Associations

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

keratosis; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

carcinoma, squamous cell; papillomavirus infections; skin neoplasms; squamous cell carcinoma; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; papillomavirus infections; skin neoplasms; squamous cell carcinoma; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; skin diseases, vesiculobullous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; skin diseases, vesiculobullous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

breast neoplasms; dna damage; lung neoplasms; mammary neoplasms; neoplasm of lung ; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; dna damage; lung neoplasms; mammary neoplasms; neoplasm of lung ; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arsenic poisoning; skin diseases Gene Set

From GAD Gene-Disease Associations

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

melanoma; neoplasms, multiple primary; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, multiple primary; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

keratosis; skin diseases Gene Set

From GAD Gene-Disease Associations

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

skin cancer; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skin cancer; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin sensitivity to sun Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skin sensitivity to sun in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

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

facial neoplasms; horse diseases; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease facial neoplasms; horse diseases; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypersensitivity; skin diseases Gene Set

From GAD Gene-Disease Associations

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

skin lesion Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; skin diseases, genetic; vitiligo Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; skin diseases, genetic; vitiligo in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperpigmentation; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

skin squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skin squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasm metastasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasm metastasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

scleroderma, systemic; skin ulcer; systemic scleroderma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease scleroderma, systemic; skin ulcer; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

scleroderma, systemic; skin ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease scleroderma, systemic; skin ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dysplastic nevus syndrome; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dysplastic nevus syndrome; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma skin cancer Gene Set

From GAD Gene-Disease Associations

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

cocarcinogenesis; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

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

skin diseases Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

microsatellite instability; nevus, pigmented; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease microsatellite instability; nevus, pigmented; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; skin diseases Gene Set

From GAD Gene-Disease Associations

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

melanoma; nevus; precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; nevus; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pulmonary; raynaud disease; scleroderma, systemic; skin ulcer; systemic scleroderma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pulmonary; raynaud disease; scleroderma, systemic; skin ulcer; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mycobacterium infections, atypical; skin ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mycobacterium infections, atypical; skin ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; cell transformation, neoplastic; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; cell transformation, neoplastic; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe photoaging of facial skin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease severe photoaging of facial skin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin Gene Set

From GeneRIF Biological Term Annotations

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

Get-1_Deficiency_GDS2629_161_mouse_embryonic skin Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the Get-1_Deficiency_GDS2629_161_mouse_embryonic skin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

regulation of water loss via skin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of water loss via skin biological process from the curated GO Biological Process Annotations dataset.

establishment of skin barrier Gene Set

From GO Biological Process Annotations

genes participating in the establishment of skin barrier biological process from the curated GO Biological Process Annotations dataset.

skin development Gene Set

From GO Biological Process Annotations

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

skin epidermis development Gene Set

From GO Biological Process Annotations

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

skin morphogenesis Gene Set

From GO Biological Process Annotations

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

skin Gene Set

From GTEx Tissue Gene Expression Profiles

genes with high or low expression in skin relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.

Skin sensitivity to sun Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Skin sensitivity to sun phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-melanoma skin cancer Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-melanoma skin cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

skin melanoma Gene Set

From GWASdb SNP-Disease Associations

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

skin cancer Gene Set

From GWASdb SNP-Disease Associations

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

skin disease Gene Set

From GWASdb SNP-Disease Associations

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

bullous skin disease Gene Set

From GWASdb SNP-Disease Associations

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

skin carcinoma Gene Set

From GWASdb SNP-Disease Associations

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

inflammatory abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

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

neoplasm of the skin Gene Set

From GWASdb SNP-Phenotype Associations

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

localized skin lesion Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin adnexa Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

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

vascular skin abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

atypical scarring of skin Gene Set

From GWASdb SNP-Phenotype Associations

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

skin rash Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

generalized abnormality of skin Gene Set

From GWASdb SNP-Phenotype Associations

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

skin Gene Set

From HPA Tissue Gene Expression Profiles

genes with high or low expression in skin relative to other tissues from the HPA Tissue Gene Expression Profiles dataset.

skin Gene Set

From HPA Tissue Protein Expression Profiles

proteins with high or low expression in skin relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.

dry skin Gene Set

From HPO Gene-Disease Associations

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

thin skin Gene Set

From HPO Gene-Disease Associations

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

telangiectases in sun-exposed and nonexposed skin Gene Set

From HPO Gene-Disease Associations

genes associated with the telangiectases in sun-exposed and nonexposed skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the skin Gene Set

From HPO Gene-Disease Associations

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

generalized abnormality of skin Gene Set

From HPO Gene-Disease Associations

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

hypopigmentation of the skin Gene Set

From HPO Gene-Disease Associations

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

abnormal delayed hypersensitivity skin test Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inflammatory abnormality of the skin Gene Set

From HPO Gene-Disease Associations

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

skin ulcer Gene Set

From HPO Gene-Disease Associations

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

punctate vasculitis skin lesions Gene Set

From HPO Gene-Disease Associations

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

profuse pigmented skin lesions Gene Set

From HPO Gene-Disease Associations

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

congenital localized absence of skin Gene Set

From HPO Gene-Disease Associations

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

excessive wrinkling of palmar skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of the skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of skin adnexa Gene Set

From HPO Gene-Disease Associations

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

postauricular skin tag Gene Set

From HPO Gene-Disease Associations

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

abnormality of the plantar skin of foot Gene Set

From HPO Gene-Disease Associations

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

diffuse skin atrophy Gene Set

From HPO Gene-Disease Associations

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

skin erosion Gene Set

From HPO Gene-Disease Associations

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

skin tags Gene Set

From HPO Gene-Disease Associations

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

vascular skin abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormal elasticity of skin Gene Set

From HPO Gene-Disease Associations

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

localized skin lesion Gene Set

From HPO Gene-Disease Associations

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

hypopigmented skin patches on arms Gene Set

From HPO Gene-Disease Associations

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

stiff skin Gene Set

From HPO Gene-Disease Associations

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

skin dimple over apex of long bone angulation Gene Set

From HPO Gene-Disease Associations

genes associated with the skin dimple over apex of long bone angulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

periauricular skin pits Gene Set

From HPO Gene-Disease Associations

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

redundant skin Gene Set

From HPO Gene-Disease Associations

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

atypical scarring of skin Gene Set

From HPO Gene-Disease Associations

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

desquamation of skin soon after birth Gene Set

From HPO Gene-Disease Associations

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

skin nodule Gene Set

From HPO Gene-Disease Associations

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

excessive wrinkled skin Gene Set

From HPO Gene-Disease Associations

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

midline skin dimples over anterior/posterior fontanelles Gene Set

From HPO Gene-Disease Associations

genes associated with the midline skin dimples over anterior/posterior fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neonatal wrinkled skin of hands and feet Gene Set

From HPO Gene-Disease Associations

genes associated with the neonatal wrinkled skin of hands and feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vasculitis in the skin Gene Set

From HPO Gene-Disease Associations

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

redundant skin on fingers Gene Set

From HPO Gene-Disease Associations

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

hyperextensible skin Gene Set

From HPO Gene-Disease Associations

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

redundant neck skin Gene Set

From HPO Gene-Disease Associations

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

preauricular skin tag Gene Set

From HPO Gene-Disease Associations

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

squamous cell carcinoma of the skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of skin morphology Gene Set

From HPO Gene-Disease Associations

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

thickened nuchal skin fold Gene Set

From HPO Gene-Disease Associations

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

premature skin wrinkling Gene Set

From HPO Gene-Disease Associations

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

abnormal blistering of the skin Gene Set

From HPO Gene-Disease Associations

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

hyperpigmentation of the skin Gene Set

From HPO Gene-Disease Associations

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

neoplasm of the skin Gene Set

From HPO Gene-Disease Associations

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

preauricular skin furrow Gene Set

From HPO Gene-Disease Associations

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

soft skin Gene Set

From HPO Gene-Disease Associations

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

hypertrophy of skin of soles Gene Set

From HPO Gene-Disease Associations

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

hypopigmented skin patches Gene Set

From HPO Gene-Disease Associations

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

warfarin-induced skin necrosis Gene Set

From HPO Gene-Disease Associations

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

skin vesicle Gene Set

From HPO Gene-Disease Associations

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

recurrent skin infections Gene Set

From HPO Gene-Disease Associations

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

skin rash Gene Set

From HPO Gene-Disease Associations

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

yellow subcutaneous tissue covered by thin, scaly skin Gene Set

From HPO Gene-Disease Associations

genes associated with the yellow subcutaneous tissue covered by thin, scaly skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lack of skin elasticity Gene Set

From HPO Gene-Disease Associations

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

fragile skin Gene Set

From HPO Gene-Disease Associations

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

skin dimples Gene Set

From HPO Gene-Disease Associations

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

depigmentation/hyperpigmentation of skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of skin physiology Gene Set

From HPO Gene-Disease Associations

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

mixed hypo- and hyperpigmentation of the skin Gene Set

From HPO Gene-Disease Associations

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

soft, doughy skin Gene Set

From HPO Gene-Disease Associations

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

regional abnormality of skin Gene Set

From HPO Gene-Disease Associations

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

recurrent bacterial skin infections Gene Set

From HPO Gene-Disease Associations

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

skin fragility with non-scarring blistering Gene Set

From HPO Gene-Disease Associations

genes associated with the skin fragility with non-scarring blistering phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

teleangiectasia of the skin Gene Set

From HPO Gene-Disease Associations

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

abnormally lax or hyperextensible skin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormally lax or hyperextensible skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

asymmetric, linear skin defects Gene Set

From HPO Gene-Disease Associations

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

thickened skin Gene Set

From HPO Gene-Disease Associations

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

skin pit Gene Set

From HPO Gene-Disease Associations

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

Skin Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Abnormalities Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Ulcer Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Diseases, Genetic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Skin Diseases, Genetic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Skin Diseases, Viral Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Skin Diseases, Viral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Galvanic Skin Response Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Galvanic Skin Response phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Skin Diseases, Parasitic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Skin Diseases, Parasitic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Skin Diseases, Vesiculobullous Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Skin Diseases, Vesiculobullous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Skin Diseases, Vascular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Skin Diseases, Vascular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Skin Diseases, Bacterial Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Skin Diseases, Bacterial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Staphylococcal Skin Infections Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Staphylococcal Skin Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Skin Diseases, Metabolic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Skin Diseases, Metabolic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Skin Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin-specific protein 32 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Skin-specific protein 32 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

dry skin Gene Set

From MPO Gene-Phenotype Associations

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

thin skin Gene Set

From MPO Gene-Phenotype Associations

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

abnormal skin condition Gene Set

From MPO Gene-Phenotype Associations

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

reddish skin Gene Set

From MPO Gene-Phenotype Associations

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

decreased skin turgor Gene Set

From MPO Gene-Phenotype Associations

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

abnormal skin exfoliation Gene Set

From MPO Gene-Phenotype Associations

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

decreased skin tensile strength Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skin tensile strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

scaly skin Gene Set

From MPO Gene-Phenotype Associations

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

blotchy skin Gene Set

From MPO Gene-Phenotype Associations

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

skin lesions Gene Set

From MPO Gene-Phenotype Associations

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

wrinkled skin Gene Set

From MPO Gene-Phenotype Associations

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

calcified skin Gene Set

From MPO Gene-Phenotype Associations

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

skin hemorrhage Gene Set

From MPO Gene-Phenotype Associations

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

abnormal skin sebaceous gland morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skin sebaceous gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

tight skin Gene Set

From MPO Gene-Phenotype Associations

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

delayed skin barrier formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed skin barrier formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

flaky skin Gene Set

From MPO Gene-Phenotype Associations

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

abnormal skin adnexa morphology Gene Set

From MPO Gene-Phenotype Associations

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

shiny skin Gene Set

From MPO Gene-Phenotype Associations

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

loose skin Gene Set

From MPO Gene-Phenotype Associations

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

skin inflammation Gene Set

From MPO Gene-Phenotype Associations

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

spontaneous skin ulceration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the spontaneous skin ulceration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skin cell number Gene Set

From MPO Gene-Phenotype Associations

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

increased sensitivity to skin irradiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sensitivity to skin irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skin adnexa physiology Gene Set

From MPO Gene-Phenotype Associations

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

impaired skin barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired skin barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

translucent skin Gene Set

From MPO Gene-Phenotype Associations

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

abnormal skin coloration Gene Set

From MPO Gene-Phenotype Associations

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

increased skin squamous cell carcinoma incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skin squamous cell carcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skin morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased sensitivity to skin irradiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased sensitivity to skin irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skin edema Gene Set

From MPO Gene-Phenotype Associations

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

abnormal skin development Gene Set

From MPO Gene-Phenotype Associations

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

skin photosensitivity Gene Set

From MPO Gene-Phenotype Associations

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

increased skin tumor incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skin tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

oily skin Gene Set

From MPO Gene-Phenotype Associations

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

abnormal skin tensile strength Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skin tensile strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skin detachment Gene Set

From MPO Gene-Phenotype Associations

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

abnormal skin turgor Gene Set

From MPO Gene-Phenotype Associations

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

thick skin Gene Set