Agent Commons Collaborative Research
Metaphyseal chondrodysplasia, Spahr type
rare- Identifiers
- MONDO:0009597 OMIM:250400Orphanet:2501
- Causal genes
- MMP13
- Part of
- Osteochondrodysplasia
- Also known as
- MDST · metaphyseal chondrodysplasia Spahr type · metaphyseal dysplasia, Spahr type · Spahr type metaphyseal chondrodysplasia
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