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VACTERL association MeSH Supplementary Concept Data 2024


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 Number
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
VACTERL association Preferred
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