MeSH Browser

MeSH Supplementary: Opitz GBBB Syndrome, X-Linked
Unique ID: C567932
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567932
Entry Term(s): Opitz BBBG Syndrome, Type I; Opitz GBBB Syndrome, Type I; Opitz Syndrome; Opitz Syndrome, X-Linked; Opitz-G Syndrome, Type I; X-Linked Opitz Syndrome (XLOS)
Heading Mapped to: *Cleft Palate; Esophagus / abnormalities; *Hypertelorism; *Hypospadias; *Genetic Diseases, X-Linked
Frequency: 14
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Concept UI: M0568232
Terms: Opitz GBBB Syndrome, X-Linked Preferred Term
Term UI T826057
Date07/12/2012
LexicalTag NON
ThesaurusID OMIM (2013); Opitz GBBB Syndrome, Type I
Term UI T826055
Date07/12/2012
LexicalTag NON
ThesaurusID OMIM (2013); Opitz Syndrome
Term UI T811378
Date11/15/2011
LexicalTag NON
ThesaurusID; Opitz BBBG Syndrome, Type I
Term UI T826056
Date07/12/2012
LexicalTag NON
ThesaurusID OMIM (2013); Opitz-G Syndrome, Type I
Term UI T811377
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); X-Linked Opitz Syndrome (XLOS)
Term UI T846265
Date06/27/2013
LexicalTag NON
ThesaurusID GHR (2014); Opitz Syndrome, X-Linked
Term UI T811379
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013)

Opitz GBBB Syndrome, X-Linked MeSH Supplementary Concept Data 2024