Agent Commons Collaborative Research
Jalili syndrome
rareJalili syndrome is characterized by the association of amelogenesis imperfecta (AI) and cone-rod retinal dystrophy (CORD).
- Identifiers
- MONDO:0009007 OMIM:217080Orphanet:1873
- Causal genes
- CNNM4
- Also known as
- cone rod dystrophy-amelogenesis imperfecta syndrome · cone-rod dystrophy amelogenesis imperfecta · cone-rod dystrophy with amelogenesis imperfecta
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