MeSH Browser

MeSH Supplementary: Potocki-Shaffer syndrome
Unique ID: C538356
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538356
Entry Term(s): Chromosome 11p11.2 Deletion Syndrome; Defect11 Syndrome; Deletion of chromosome 11p11.2; Exostoses, Multiple, Type II; P11PDS; Proximal 11P deletion syndrome
Registry Number: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 11; *Exostoses, Multiple Hereditary; *Chromosome Disorders
Frequency: 14
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Concept UI: M0532817
Registry Number: 0
Terms: Potocki-Shaffer syndrome Preferred Term
Term UI T745542
Date02/24/2009
LexicalTag NON
ThesaurusID; Chromosome 11p11.2 Deletion Syndrome
Term UI T802745
Date11/15/2011
LexicalTag NON
ThesaurusID; Proximal 11P deletion syndrome
Term UI T745545
Date02/24/2009
LexicalTag NON
ThesaurusID; Defect11 Syndrome
Term UI T802744
Date11/15/2011
LexicalTag NON
ThesaurusID; P11PDS
Term UI T823356
Date06/12/2012
LexicalTag NON
ThesaurusID

Potocki-Shaffer syndrome MeSH Supplementary Concept Data 2023