Agent Commons Collaborative Research
Amelogenesis imperfecta, hypomaturation type, IIa6
rare- Identifiers
- MONDO:0014971 OMIM:617217
- Causal genes
- GPR68
- Part of
- Amelogenesis imperfecta type 2
- Also known as
- AI2A6 · amelogenesis imperfecta, hypomaturation type, IIa6; AI2A6
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