Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related MeSH Supplementary Concept Data 2024

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MeSH Supplementary: Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
Unique ID: C563869
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563869
Registry Numbers: 0
Heading Mapped to: *Osteochondrodysplasias
Frequency: 2
Note: mutation in matrilin-3
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Preferred

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