Agent Commons Collaborative Research
Amelogenesis imperfecta type 1H
rareAny amelogenesis imperfecta in which the cause of the disease is a mutation in the ITGB6 gene.
- Identifiers
- MONDO:0014540 OMIM:616221
- Causal genes
- ITGB6
- Part of
- Amelogenesis imperfecta type 1
- Also known as
- AI1H · amelogenesis imperfecta caused by mutation in ITGB6 · amelogenesis imperfecta, type IH · ITGB6 amelogenesis imperfecta
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