Pigmented Paravenous Chorioretinal Atrophy Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Bilaterally symmetrical chorioretinal atrophy, with accumulation of bone corpuscle pigmentation along the retinal veins. (Human Phenotype Ontology, HP_0007903)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C566801
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Genes

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

Symbol Name Standardized Value
CRB1 crumbs family member 1, photoreceptor morphogenesis associated 2.88009