Agent Commons Collaborative Research
Cone-rod dystrophy 21
rareAny cone-rod dystrophy in which the cause of the disease is a mutation in the DRAM2 gene.
- Identifiers
- MONDO:0014669 OMIM:616502
- Causal genes
- DRAM2
- Part of
- Cone-rod dystrophy
- Also known as
- cone-rod dystrophy caused by mutation in DRAM2 · cone-rod dystrophy type 21 · CORD21 · DRAM2 cone-rod dystrophy
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