MeSH Browser

MeSH Supplementary: 9q22.3 Microdeletion
Unique ID: C579873
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C579873
Entry Term(s): 9q22 Deletion Syndrome; 9q22.3 Deletion; Microdeletion 9q22.3 Syndrome
Registry Number: 0
Heading Mapped to: Chromosomes, Human, Pair 9; *Chromosome Disorders
Frequency: 6
Date of Entry: 2013/10/24
Revision Date: 2016/07/07

Concept UI: M0583319
Registry Number: 0
Terms: 9q22.3 Microdeletion Preferred Term
Term UI T840803
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); 9q22.3 Deletion
Term UI T840805
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Microdeletion 9q22.3 Syndrome
Term UI T840806
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); 9q22 Deletion Syndrome
Term UI T840804
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

9q22.3 Microdeletion MeSH Supplementary Concept Data 2023