MeSH Browser

MeSH Supplementary: VACTERL association
Unique ID: C536495
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536495
Entry Term(s): VACTEL Association; VACTERL Syndrome; Vertebral Anal Tracheoesophageal Esophageal Radial anomalies
Registry Numbers: 0
Heading Mapped to: Anal Canal / abnormalities; Esophagus / abnormalities; *Heart Defects, Congenital; Kidney / abnormalities; Spine / abnormalities; Trachea / abnormalities; *Limb Deformities, Congenital
Frequency: 189
Note: An association of congenital abnormalities: vertebral defects (V), ANAL ATRESIA (A), cardiac malformations (C) TRACHEOESOPHAGEAL FISTULA with ESOPHAGEAL ATRESIA (TE), radial or renal dysplasia (R), and limb anomalies (L). A heterozygous mutation in the HOXD13 gene has been identified. OMIM: 192350
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Concept UI: M0530956
Registry Numbers: 0
Terms: VACTERL association Preferred Term
Term UI T739518
Date02/24/2009
LexicalTag NON
ThesaurusID; Vertebral Anal Tracheoesophageal Esophageal Radial anomalies
Term UI T739520
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); VACTEL Association
Term UI T739521
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); VACTERL Syndrome
Term UI T739522
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

VACTERL association MeSH Supplementary Concept Data 2025