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Amelogenesis imperfecta type 2A1
rareAny amelogenesis imperfecta in which the cause of the disease is a mutation in the KLK4 gene.
- Identifiers
- MONDO:0008772 OMIM:204700
- Causal genes
- KLK4
- Part of
- Amelogenesis imperfecta type 2
- Also known as
- AI2A1 · amelogenesis imperfecta caused by mutation in KLK4 · amelogenesis imperfecta pigmented hypomaturation type · amelogenesis imperfecta, hypomaturation type, IIA1 · amelogenesis imperfecta, pigmented hypomaturation type, 1
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