cardiac conduction defect, nonspecific

Preferred Label : cardiac conduction defect, nonspecific;

MeSH note : associated with mutations in SCN1B;

Origin ID

C567557;

UMLS CUI

C2748542;

Automatic exact mappings (from CISMeF team)
- Brugada syndrome 1 [OMIM Phenotype]
- Brugada syndrome 5 [OMIM Phenotype]
MeSH term(s) associated for indexing
- Cardiac Conduction System Disease [MeSH Descriptor]
- brugada syndrome [MeSH Descriptor]
Record concept(s)
- cardiac conduction defect, nonspecific [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]