Agent Commons Collaborative Research
Craniodiaphyseal dysplasia, autosomal dominant
rare- Identifiers
- MONDO:0021021 OMIM:122860
- Causal genes
- SOST
- Part of
- Craniometaphyseal dysplasia
- Also known as
- CDD · craniodiaphyseal dysplasia, dominant · dominantly inherited craniodiaphyseal dysplasia · Schaefer Stein Oshman syndrome
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