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Spondyloepimetaphyseal Dysplasia, X-Linked MeSH Supplementary Concept Data 2023


MeSH Supplementary
Spondyloepimetaphyseal Dysplasia, X-Linked
Unique ID
C564714
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C564714
Entry Term(s)
SEMD, X-Linked
Registry Number
0
Heading Mapped to
*Osteochondrodysplasias
*Genetic Diseases, X-Linked
Frequency
2
Date of Entry
2012/11/05
Spondyloepimetaphyseal Dysplasia, X-Linked Preferred
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