Brugada syndrome 3

Preferred Label : Brugada syndrome 3;

Symbol : BRGDA3;

CISMeF acronym : BRGDA3;

Type : Phenotype, molecular basis known;

Prefixed ID : #611875;

Details

Origin ID

611875;

UMLS CUI

C2678478;

Currated CISMeF NLP mapping
- Brugada syndrome 3 [DO Concept]
- brugada syndrome 3 [MeSH concept]
- brugada syndrome 3 [MeSH Supplementary Concept]
DO Cross reference
- Brugada syndrome 3 [DO Concept]
Genes related to phenotype
- Calcium channel, voltage-dependent, L type, alpha-1c subunit [OMIM gene]
HPO term(s)
- Atrial fibrillation [HPO term]
- Autosomal dominant inheritance [HPO term]
- J wave [HPO term]
- Shortened QT interval [HPO term]
- Sudden cardiac death [HPO term]
- Syncope [HPO term]
- Ventricular arrhythmia [HPO term]
ORDO concept(s)
- Brugada syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Brugada syndrome 3 [DO Concept]
- brugada syndrome 3 [MeSH Supplementary Concept]
- brugada syndrome 3 [MeSH concept]
Validated automatic mappings to NTBT
- Brugada syndrome [ORDO Disease]

Keyword's position in hierarchy(ies) :

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