MeSH Browser

MeSH Supplementary: Chromosome 17 trisomy
Unique ID: C538044
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538044
Entry Term(s): Chromosome 17 duplication; Trisomy 17; Trisomy 17 mosaicism
Registry Numbers: 0
Heading Mapped to: Chromosomes, Human, Pair 17; Mosaicism; *Trisomy
Frequency: 36
Note: Duplication of chromosome 17 in some tissues (trisomy 17 mosaicism) is among the rarest trisomy in humans and full trisomy 17 has never been observed in living individuals. In mosaic cases, where trisomy occurs only in some cell populations, affected individuals may experience developmental delays, body asymmetry, slow growth, and cerebellar hypoplasia.
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Concept UI: M0532505
Registry Numbers: 0
Terms: Chromosome 17 trisomy Preferred Term
Term UI T744578
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Trisomy 17 mosaicism
Term UI T744579
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Chromosome 17 duplication
Term UI T744580
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Trisomy 17
Term UI T744581
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Chromosome 17 trisomy MeSH Supplementary Concept Data 2025