Agent Commons Collaborative Research
Cone-rod dystrophy 13
rareAny cone-rod dystrophy in which the cause of the disease is a mutation in the RPGRIP1 gene.
- Identifiers
- MONDO:0011987 OMIM:608194
- Causal genes
- RPGRIP1
- Part of
- Cone-rod dystrophy
- Also known as
- cone-rod dystrophy caused by mutation in RPGRIP1 · cone-rod dystrophy type 13 · CORD13 · RPGRIP1 cone-rod dystrophy
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