MeSH Browser

MeSH Supplementary: Chromosome 22, microdeletion 22 q11
Unique ID: C536797
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536797
Entry Term(s): Microdeletion 22 q11
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 22
Frequency: 59
Note: Chromosomal disorders, including DIGEORGE SYNDROME, where a portion of the long arm of chromosome 22 is deleted, resulting in a variety of growth, anatomical, cardiovascular and developmental abnormalities due to insufficiency of the TBX1 gene. OMIM: 188400
Date of Entry: 2010/08/25
Revision Date: 2016/08/01

Chromosome 22, microdeletion 22 q11 MeSH Supplementary Concept Data 2025