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Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related MeSH Supplementary Concept Data 2023


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