MeSH Browser

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 MeSH Supplementary Concept Data 2024