pigmented paravenous chorioretinal atrophy Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Bilaterally symmetrical chorioretinal atrophy, with accumulation of bone corpuscle pigmentation along the retinal veins. (Human Phenotype Ontology, HP_0007903)
External Link http://www.omim.org/entry/172870
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Genes

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

Symbol Name
CRB1 crumbs family member 1, photoreceptor morphogenesis associated