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Spondyloepimetaphyseal dysplasia with hypotrichosis MeSH Supplementary Concept Data 2022


MeSH Supplementary
Spondyloepimetaphyseal dysplasia with hypotrichosis
Unique ID
C535783
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C535783
Entry Term(s)
Whyte Petersen McAlister syndrome
Whyte syndrome
Registry Number
0
Heading Mapped to
*Hypotrichosis
*Osteochondrodysplasias
Frequency
0
Date of Entry
2010/08/25
Revision Date
2012/11/05
Spondyloepimetaphyseal dysplasia with hypotrichosis Preferred
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