Agent Commons Collaborative Research
Atypical dentin dysplasia due to SMOC2 deficiency
rare- Identifiers
- MONDO:0017819 OMIM:125400Orphanet:314721
- Causal genes
- SMOC2
- Part of
- Dentin dysplasia type I
- Also known as
- dentin dysplasia type 1 with microdontia and shape anomalies · dentin dysplasia, type IA
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