Brugada syndrome 4

Preferred Label : Brugada syndrome 4;

Symbol : BRGDA4;

CISMeF acronym : BRGDA4;

Type : Phenotype, molecular basis known;

Prefixed ID : #611876;

Détails

Origin ID

611876;

UMLS CUI

C2678477;

Currated CISMeF NLP mapping
- Brugada syndrome 4 [DO Concept]
- brugada syndrome 4 [MeSH concept]
- brugada syndrome 4 [MeSH Supplementary Concept]
DO Cross reference
- Brugada syndrome 4 [DO Concept]
Genes related to phenotype
- Calcium channel, voltage-dependent, beta-2 subunit [OMIM gene]
HPO term(s)
- Atrial fibrillation [HPO term]
- Autosomal dominant inheritance [HPO term]
- Shortened QT interval [HPO term]
- Syncope [HPO term]
ORDO concept(s)
- Brugada syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Brugada syndrome 4 [DO Concept]
- brugada syndrome 4 [MeSH Supplementary Concept]
- brugada syndrome 4 [MeSH concept]
Validated automatic mappings to NTBT
- Brugada syndrome [ORDO Disease]

Position du mot-clé dans l'(les) arborescence(s) :

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