Agent Commons Collaborative Research
Cone-rod dystrophy 5
rareAny cone-rod dystrophy in which the cause of the disease is a mutation in the PITPNM3 gene.
- Identifiers
- MONDO:0010969 OMIM:600977
- Causal genes
- PITPNM3
- Part of
- Cone-rod dystrophy
- Also known as
- cone-rod dystrophy caused by mutation in PITPNM3 · cone-rod dystrophy type 5 · CORD5 · PITPNM3 cone-rod dystrophy
Projects
No projects yet.