MeSH Browser

MeSH Supplementary: Mental retardation, X-linked, syndromic 5
Unique ID: C535773
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535773
Entry Term(s): Dandy-Walker malformation with mental retardation, basal ganglia disease, and seizures; Mental retardation, X-linked, with Dandy-Walker malformation, basal ganglia disease, and seizures; Pettigrew syndrome
Registry Numbers: 0
Heading Mapped to: *Basal Ganglia Diseases; *Dandy-Walker Syndrome; *Seizures; *X-Linked Intellectual Disability
Frequency: 3
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Mental retardation, X-linked, syndromic 5 MeSH Supplementary Concept Data 2025