Spondyloepimetaphyseal Dysplasia, Pakistani Type MeSH Supplementary Concept Data 2024

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MeSH Supplementary: Spondyloepimetaphyseal Dysplasia, Pakistani Type
Unique ID: C567551
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567551
Entry Term(s): SEMD, Pakistani Type
Registry Number: 0
Heading Mapped to: *Growth Disorders; *Osteochondrodysplasias
Frequency: 1
Note: mutation in PAPSS2
Date of Entry: 2012/11/05

Spondyloepimetaphyseal Dysplasia, Pakistani Type Preferred

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