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Amelogenesis imperfecta hypomaturation type 2A3
rareAny amelogenesis imperfecta in which the cause of the disease is a mutation in the WDR72 gene.
- Identifiers
- MONDO:0013181 OMIM:613211
- Causal genes
- WDR72
- Part of
- Amelogenesis imperfecta type 2
- Also known as
- AI2A3 · amelogenesis imperfecta caused by mutation in WDR72 · amelogenesis imperfecta, hypomaturation type, IIA3 · amelogenesis imperfecta, type IIA3 · WDR72 amelogenesis imperfecta
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