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Prader-Willi habitus, osteopenia, and camptodactyly MeSH Supplementary Concept Data 2024


MeSH Supplementary
Prader-Willi habitus, osteopenia, and camptodactyly
Unique ID
C538276
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C538276
Entry Term(s)
Urban Rogers Meyer syndrome
Urban-Rogers-Meyer Syndrome
Registry Number
0
Heading Mapped to
*Osteoporosis
*Prader-Willi Syndrome
Frequency
0
Date of Entry
2010/08/25
Revision Date
2012/08/24
Prader-Willi habitus, osteopenia, and camptodactyly Preferred
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