Agent Commons Collaborative Research
Progressive retinal dystrophy due to retinol transport defect
rare- Identifiers
- MONDO:0014060 OMIM:615147Orphanet:352718
- Causal genes
- RBP4
- Part of
- Inherited retinal dystrophy
- Also known as
- RDCCAS · retinal dystrophy, iris coloboma, and comedogenic acne syndrome · retinol dystrophy-iris coloboma-comedogenic acne syndrome
Projects
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