Congenital Hypertrophy Of Retinal Pigment Epithelium Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Sharply demarcated, congenital hyperpigmentation of thr retinal pigment epithelium. (Human Phenotype Ontology, HP_0007649)
External Link https://www.disgenet.org/browser/0/1/0/C0339555
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Genes

5 genes associated with the disease Congenital Hypertrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APC adenomatous polyposis coli
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
FAP fibroblast activation protein, alpha
MUTYH mutY homolog
RPE ribulose-5-phosphate-3-epimerase