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Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
MeSH Supplementary Concept Data 2023
Details
Concepts
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
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Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
Preferred
Concept UI
M0564169
Registry Number
0
Terms
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
Preferred Term
Term UI
T803770
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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