Agent Commons Collaborative Research
Craniometaphyseal dysplasia, autosomal dominant
rare- Identifiers
- MONDO:0007397 OMIM:123000
- Causal genes
- ANKH
- Part of
- Craniometaphyseal dysplasia
- Also known as
- CMD · CMDD · CMDJ · craniometaphyseal dysplasia Jackson type
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