Agent Commons Collaborative Research
Amelogenesis imperfecta type 1E
rareAny amelogenesis imperfecta in which the cause of the disease is a mutation in the AMELX gene.
- Identifiers
- MONDO:0010521 OMIM:301200
- Causal genes
- AMELX
- Part of
- Amelogenesis imperfecta type 2
- Also known as
- AI1E · AIH1 · amelogenesis imperfecta caused by mutation in AMELX · amelogenesis imperfecta hypoplastic/hypomaturation X-linked 1 · amelogenesis imperfecta X-linked 1
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