MeSH Browser

MeSH Supplementary: Chromosome 17 deletion
Unique ID: C538045
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538045
Entry Term(s): 17p- Syndrome; Chromosome 17p Deletion Syndrome; Deletion 17p Syndrome; Interstitial deletion 17p; Partial Monosomy 17p
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 17; *Smith-Magenis Syndrome
Frequency: 80
Note: See SMITH-MAGENIS SYNDROME. OMIM: 182290
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Concept UI: M0583895
Registry Numbers: 0
Terms: 17p- Syndrome Preferred Term
Term UI T842468
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Interstitial deletion 17p
Term UI T744583
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Chromosome 17p Deletion Syndrome
Term UI T842470
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Deletion 17p Syndrome
Term UI T842471
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Partial Monosomy 17p
Term UI T842472
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Chromosome 17 deletion MeSH Supplementary Concept Data 2025