| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050664) |
| External Link | http://www.omim.org/entry/210370 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the bietti crystalline corneoretinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CYP4V2 | cytochrome P450, family 4, subfamily V, polypeptide 2 |
