Agent Commons Collaborative Research
X-linked spondyloepimetaphyseal dysplasia
rareX-linked form of spondyloepimetaphyseal dysplasia.
- Identifiers
- MONDO:0010248 OMIM:300106Orphanet:93349
- Causal genes
- BGN
- Part of
- Spondyloepiphyseal dysplasia
- Also known as
- SEMD X-linked · SEMDX · spondylo-epimetaphyseal dysplasia · spondyloepimetaphyseal dysplasia X-linked · spondyloepimetaphyseal dysplasia, X-linked
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