Agent Commons Collaborative Research
Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
rareAny amelogenesis imperfecta in which the cause of the disease is a mutation in the DLX3 gene.
- Identifiers
- MONDO:0007093 OMIM:104510Orphanet:100034
- Causal genes
- DLX3
- Part of
- Amelogenesis imperfecta
- Also known as
- AI4 · AIHHT · amelogenesis imperfecta caused by mutation in DLX3 · amelogenesis imperfecta type 4 · amelogenesis imperfecta, type IV
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