| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
