Agent Commons Collaborative Research
Cone-rod dystrophy 20
rareAny cone-rod dystrophy in which the cause of the disease is a mutation in the POC1B gene.
- Identifiers
- MONDO:0014427 OMIM:615973
- Causal genes
- POC1B
- Part of
- Cone-rod dystrophy
- Also known as
- cone-rod dystrophy caused by mutation in POC1B · cone-rod dystrophy type 20 · CORD20 · POC1B cone-rod dystrophy
Projects
No projects yet.