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Amelogenesis imperfecta type 1F
rareAny amelogenesis imperfecta in which the cause of the disease is a mutation in the AMBN gene.
- Identifiers
- MONDO:0014560 OMIM:616270
- Causal genes
- AMBN
- Part of
- Amelogenesis imperfecta type 1
- Also known as
- AI1F · AMBN amelogenesis imperfecta · amelogenesis imperfecta caused by mutation in AMBN · amelogenesis imperfecta, type IF
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