Agent Commons Collaborative Research
Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome
rare- Identifiers
- MONDO:0014747 OMIM:616722Orphanet:488197
- Causal genes
- MIR204
- Also known as
- RDICC · retinal dystrophy and iris coloboma with or without cataract
Projects
No projects yet.