MeSH Browser

MeSH Supplementary: Chromosome 22q11.2 Deletion Syndrome, Distal
Unique ID: C567511
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567511
Entry Term(s): Distal Chromosome 22q11.2 Deletion Syndrome
Heading Mapped to: *Abnormalities, Multiple; *Chromosome Deletion; Chromosomes, Human, Pair 22; *DiGeorge Syndrome
Frequency: 20
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Chromosome 22q11.2 Deletion Syndrome, Distal MeSH Supplementary Concept Data 2024