Spondyloepimetaphyseal Dysplasia, X-Linked MeSH Supplementary Concept Data 2024

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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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