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Amelogenesis imperfecta hypomaturation type 2A2
rareAny amelogenesis imperfecta in which the cause of the disease is a mutation in the MMP20 gene.
- Identifiers
- MONDO:0012926 OMIM:612529
- Causal genes
- MMP20
- Part of
- Amelogenesis imperfecta type 2
- Also known as
- AI2A2 · amelogenesis imperfecta caused by mutation in MMP20 · amelogenesis imperfecta, hypomaturation type, IIA2 · amelogenesis imperfecta, type IIA2 · MMP20 amelogenesis imperfecta
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