MeSH Browser

MeSH Supplementary: Chromosome Xq28 Duplication Syndrome
Unique ID: C567580
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567580
Entry Term(s): Gdi1 Duplication Syndrome
Registry Numbers: 0
Heading Mapped to: *Intellectual Disability; *Facies; *Craniofacial Abnormalities; *Sex Chromosome Disorders; *Genetic Diseases, X-Linked; *Chromosome Duplication
Frequency: 4
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Chromosome Xq28 Duplication Syndrome MeSH Supplementary Concept Data 2025