Name

PBCRA1 Gene

progressive bifocal chorioretinal atrophy 1

chorioretinal hypopigmentation or hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.

Hypopigmentation Gene Set

From CTD Gene-Disease Associations

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

Yemenite deaf-blind hypopigmentation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Yemenite deaf-blind hypopigmentation syndrome from the curated CTD Gene-Disease Associations dataset.

hypopigmentation Gene Set

From GeneRIF Biological Term Annotations

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

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.

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.

spotty hypopigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the spotty hypopigmentation 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.

generalized hypopigmentation Gene Set

From HPO Gene-Disease Associations

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

iris hypopigmentation Gene Set

From HPO Gene-Disease Associations

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

hypopigmentation of the fundus Gene Set

From HPO Gene-Disease Associations

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

Hypopigmentation Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

hypopigmentation Gene Set

From MPO Gene-Phenotype Associations

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

Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sveinsson Chorioretinal Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sveinsson Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.

Chorioretinal atrophy, progressive bifocal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset.

Pigmented Paravenous Chorioretinal Atrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pigmented Paravenous Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.

chorioretinal scar Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

chorioretinal Gene Set

From GeneRIF Biological Term Annotations

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

chorioretinal abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

chorioretinal abnormality Gene Set

From HPO Gene-Disease Associations

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

chorioretinal dysplasia Gene Set

From HPO Gene-Disease Associations

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

peripapillary chorioretinal atrophy Gene Set

From HPO Gene-Disease Associations

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

chorioretinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

chorioretinal coloboma Gene Set

From HPO Gene-Disease Associations

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

pigmented paravenous chorioretinal atrophy Gene Set

From HPO Gene-Disease Associations

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

chorioretinal atrophy Gene Set

From HPO Gene-Disease Associations

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

microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated OMIM Gene-Disease Associations dataset.

pigmented paravenous chorioretinal atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the pigmented paravenous chorioretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

Hyperpigmentation, familial progressive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperpigmentation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperpigmentation from the curated CTD 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.

hyperpigmentation Gene Set

From GAD Gene-Disease Associations

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

hyperpigmentation Gene Set

From GeneRIF Biological Term Annotations

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

spotty hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

macular hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

hyperpigmentation in sun-exposed areas Gene Set

From HPO Gene-Disease Associations

genes associated with the hyperpigmentation in sun-exposed areas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive reticulate hyperpigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive reticulate hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lip hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

generalized hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

hyperpigmentation of the fundus Gene Set

From HPO Gene-Disease Associations

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

progressive hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

linear hyperpigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the linear hyperpigmentation 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.

periorbital hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

reticular hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

forehead hyperpigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the forehead hyperpigmentation 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.

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.

irregular hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

foveal hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

Hyperpigmentation Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

hyperpigmentation Gene Set

From MPO Gene-Phenotype Associations

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

hyperpigmentation, familial progressive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperpigmentation, familial progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.