MeSH Browser

MeSH Supplementary: Spondylometaphyseal dysplasia, Algerian type
Unique ID: C535794
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535794
Entry Term(s): Spondylometaphyseal Dysplasia With Severe Genu Valgum; Spondylometaphyseal Dysplasia, Schmidt Type
Registry Numbers: 0
Heading Mapped to: *Osteochondrodysplasias
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Spondylometaphyseal dysplasia, Algerian type MeSH Supplementary Concept Data 2025