MeSH Browser

MeSH Supplementary: Opitz-Kaveggia syndrome
Unique ID: C537923
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537923
Entry Term(s): FG syndrome; FG syndrome 1; FG syndrome 2; FG syndrome 3; FG syndrome 4; FGS1; Keller syndrome; Mental Retardation, Large Head, Imperforate Anus, Congenital Hypotonia, and Partial Agenesis of the Corpus Callosum; Mental Retardation, X-Linked, Cask-Related; Mental Retardation, X-Linked, With Nystagmus
Registry Numbers: 0
Heading Mapped to: *Anus, Imperforate; *Constipation; Muscle Hypotonia / congenital; *X-Linked Intellectual Disability; *Agenesis of Corpus Callosum
Frequency: 12
Note: Mental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum.
Source: Z Kinderheilkd. 117(1):1-18
Date of Entry: 2010/08/25
Revision Date: 2021/05/20

Opitz-Kaveggia syndrome MeSH Supplementary Concept Data 2025