| Human Disease |
Term: Spondyloepimetaphyseal Dysplasia, Strudwick Type; SEMDSTWK
OMIM ID: 184250
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| Synonyms |
Dappled Metaphysis Syndrome; Semdc; SEMD, Strudwick Type; SMED, Strudwick Type; SMED, Type I; Spondylometaepiphyseal Dysplasia Congenita, Strudwick Type; Spondylometaphyseal Dysplasia; SMD; Strudwick Syndrome |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
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Characteristics of this human disease are associated with mutations in... |
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 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
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Analysis Tools