|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Bilaterally symmetrical chorioretinal atrophy, with accumulation of bone corpuscle pigmentation along the retinal veins. (Human Phenotype Ontology, HP_0007903)|
|Downloads & Tools|
1 genes associated with the pigmented paravenous chorioretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
|CRB1||crumbs family member 1, photoreceptor morphogenesis associated|