Atrial fibrillation, familial, 7

Preferred Label : Atrial fibrillation, familial, 7;

Symbol : ATFB7;

CISMeF acronym : ATFB7;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the potassium channel, voltage-gated, shaker-related subfamily, member 5 gene (KCNA5, 176267.0001);

Prefixed ID : #612240;

Details

Origin ID

612240;

UMLS CUI

C2677106;

Broader ORDO disease(s)
- Familial atrial fibrillation [ORDO Disease]
Currated CISMeF NLP mapping
- atrial fibrillation, familial, 7 [MeSH concept]
- atrial fibrillation, familial, 7 [MeSH Supplementary Concept]
DO Cross reference
- familial atrial fibrillation [DO Concept]
Genes related to phenotype
- Potassium channel, voltage-gated, shaker-related subfamily, member 5 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Palpitations [HPO term]
- Paroxysmal atrial fibrillation [HPO term]
- Prolonged PR interval [HPO term]
- Prolonged QTc interval [HPO term]
ORDO concept(s)
- Familial atrial fibrillation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- atrial fibrillation, familial, 7 [MeSH Supplementary Concept]
- atrial fibrillation, familial, 7 [MeSH concept]
Validated automatic mappings to NTBT
- Familial atrial fibrillation [ORDO Disease]
- familial atrial fibrillation [DO Concept]

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