MeSH Browser

MeSH Supplementary: Hereditary bundle branch system defect
Unique ID: C566873
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566873
Entry Term(s): Cardiac conduction defect, progressive; Heart Block, Progressive Familial, Type I; Heart block progressive, familial; Heart block, progressive familial, type 1; Lenegre Lev disease; Lenegre-Lev Disease; Pfhb1a; PfhbIa; Pfhbi; Progressive Familial Heart Block, Type Ia
Registry Numbers: 0
Heading Mapped to: *Heart Block; *Cardiac Conduction System Disease
Frequency: 378
Note: A form of heart block caused by dominant mutations in the SCN5A gene and characterized by RIGHT BUNDLE-BRANCH BLOCK. OMIM: 113900
Date of Entry: 2012/11/05
Revision Date: 2017/09/22

Concept UI: M0530309
Registry Numbers: 0
Terms: Hereditary bundle branch system defect Preferred Term
Term UI T737422
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Heart block, progressive familial, type 1
Term UI T737418
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Cardiac conduction defect, progressive
Term UI T737420
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Lenegre Lev disease
Term UI T737424
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Progressive Familial Heart Block, Type Ia
Term UI T809309
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Lenegre-Lev Disease
Term UI T809310
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Heart Block, Progressive Familial, Type I
Term UI T809311
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Pfhb1a
Term UI T809312
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Pfhbi
Term UI T809315
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Heart block progressive, familial
Term UI T737417
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); PfhbIa
Term UI T831198
Date10/12/2012
LexicalTag NON
ThesaurusID OMIM (2013)

Hereditary bundle branch system defect MeSH Supplementary Concept Data 2025