MeSH Browser

MeSH Supplementary: 7p2 monosomy syndrome
Unique ID: C537818
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537818
Entry Term(s): Chromosome 7, monosomy 7p2; Chromosome 7, partial deletion of short arm (7p2-); Chromosome 7, partial monosomy 7p; Chromosome 7, terminal 7p deletion (del 7p21-p22)
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 7; *Chromosome Disorders
Frequency: 0
Date of Entry: 2010/06/25
Revision Date: 1955/01/01

7p2 monosomy syndrome MeSH Supplementary Concept Data 2025