Brugada syndrome 6

Preferred Label : Brugada syndrome 6;

Symbol : BRGDA6;

CISMeF acronym : BRGDA6;

Type : Phenotype, molecular basis known;

Prefixed ID : #613119;

Details

Origin ID

613119;

UMLS CUI

C2751089;

Currated CISMeF NLP mapping
- Brugada syndrome 6 [DO Concept]
- brugada syndrome 6 [MeSH concept]
- brugada syndrome 6 [MeSH Supplementary Concept]
DO Cross reference
- Brugada syndrome 6 [DO Concept]
Genes related to phenotype
- Potassium channel, voltage-gated, isk-related subfamily, member 3 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Cardiac arrest [HPO term]
- ST segment elevation [HPO term]
- Ventricular fibrillation [HPO term]
ORDO concept(s)
- Brugada syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Brugada syndrome 6 [DO Concept]
- brugada syndrome 6 [MeSH Supplementary Concept]
- brugada syndrome 6 [MeSH concept]
Validated automatic mappings to NTBT
- Brugada syndrome [ORDO Disease]

Keyword's position in hierarchy(ies) :

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