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Weaver syndrome MeSH Supplementary Concept Data 2024


MeSH Supplementary
Weaver syndrome
Unique ID
C536687
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C536687
Entry Term(s)
Weaver Smith syndrome
Weaver-Smith Syndrome
Registry Number
0
Heading Mapped to
*Abnormalities, Multiple
*Congenital Hypothyroidism
*Hand Deformities, Congenital
*Craniofacial Abnormalities
Frequency
29
Note
Overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly
Date of Entry
2010/08/25
Revision Date
2012/08/24
Weaver syndrome Preferred
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