MeSH Browser

MeSH Supplementary: Chromosome 7, monosomy
Unique ID: C537814
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537814
Entry Term(s): Monosomy 7
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 7
Frequency: 104
Note: Conditions associated with loss of segments of chromosome 7, such as WILLIAMS SYNDROME, resulting in growth abnormalities, intellectual disability, and immunologic disorders.
Date of Entry: 2010/08/25
Revision Date: 2016/08/01

Chromosome 7, monosomy MeSH Supplementary Concept Data 2025