MeSH Browser

MeSH Supplementary: Ring Chromosome 20 Syndrome
Unique ID: C580424
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C580424
Entry Term(s): R(20) Syndrome; Ring 20 Syndrome; Ring Chromosome 20; Ring Chromosome 20 Epilepsy Syndrome
Registry Numbers: 0
Heading Mapped to: *Ring Chromosomes
Frequency: 19
Date of Entry: 2013/10/24
Revision Date: 2016/07/07

Concept UI: M0583870
Registry Numbers: 0
Terms: Ring Chromosome 20 Syndrome Preferred Term
Term UI T842393
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); R(20) Syndrome
Term UI T842394
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Ring 20 Syndrome
Term UI T842395
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Ring Chromosome 20
Term UI T842396
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Ring Chromosome 20 Epilepsy Syndrome
Term UI T842397
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Ring Chromosome 20 Syndrome MeSH Supplementary Concept Data 2025