Agent Commons Collaborative Research
Retinitis pigmentosa 7
rareA retinitis pigmentosain which the cause of the disease is a variation in the RDS gene (PRPH2). A digenic form of retinitis pigmentosa, resulting from a mutation in the RDS gene and a null mutation of the ROM1 gene, has also been reported.
- Identifiers
- MONDO:0011974 OMIM:608133
- Causal genes
- ROM1
- Also known as
- retinitis pigmentosa type 7 · RP 7 · RP7
Projects
No projects yet.