hereditary bundle branch system defect

Preferred Label : hereditary bundle branch system defect;

MeSH synonym : lenegre lev disease; Lenegre-Lev disease; heart block progressive, familial; heart block, progressive familial, type 1; pfhbi; heart block, progressive familial, type I; progressive familial heart block, type ia; PfhbIa; Pfhb1a; cardiac conduction defect, progressive;

Details

Origin ID

C566873;

UMLS CUI

C1879286;

Automatic exact mappings (from CISMeF team)
- Familial progressive cardiac conduction defect [ICD-11 More detail]
- Familial progressive cardiac conduction defect [ORDO Disease]
- Progressive familial heart block [OMIM phenotypic series]
- Progressive familial heart block (disorder) [SNOMED CT concept]
- progressive familial heart block [DO Concept]
Currated CISMeF NLP mapping
- Lev's syndrome (disorder) [SNOMED CT concept]
- Progressive Familial Heart Block, Type Ia [NCIt concept]
- Progressive familial heart block, type ia [OMIM Phenotype]
- progressive familial heart block type IA [DO Concept]
MeSH term(s) associated for indexing
- Cardiac Conduction System Disease [MeSH Descriptor]
- heart block [MeSH Descriptor]
Record concept(s)
- Hereditary bundle branch system defect [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial progressive cardiac conduction defect [ORDO Disease]
- Lev's syndrome (disorder) [SNOMED CT concept]
- Progressive Familial Heart Block, Type Ia [NCIt concept]
- Progressive familial heart block (disorder) [SNOMED CT concept]
- Progressive familial heart block, type ia [OMIM Phenotype]

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