Summary

Pigmented Paravenous Chorioretinal Atrophy, also known as pigmented paravenous retinochoroidal atrophy,is related to chorioretinitis and retinitis,and has symptoms including hypermetropia, esotropia and vitreoretinal degeneration. An important gene associated with Pigmented Paravenous Chorioretinal Atrophy is CRB1 (Crumbs 1, Cell Polarity Complex Component). Affiliated tissues include bone, retina and eye

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Symptoms Associated With Trait