MeSH Browser

MeSH Supplementary: Atrioventricular Septal Defect
Unique ID: C562831
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562831
Entry Term(s): AVC Defect; AVSD; Atrioventricular Canal Defect
Registry Number: 0
Heading Mapped to: *Heart Septal Defects
Frequency: 326
Note: A range of congenital heart septal defects characterized by both a common atrioventricular junction and deficient atrioventricular septation. Germline mutations in the COL6A1, COL6A2, and CRELD1 genes have been identified. OMIM: 606215
Date of Entry: 2012/11/05
Revision Date: 2015/08/17

Atrioventricular Septal Defect MeSH Supplementary Concept Data 2024