Atrial fibrillation, familial, 10

Preferred Label : Atrial fibrillation, familial, 10;

Symbol : ATFB10;

CISMeF acronym : ATFB10;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the sodium channel, voltage-gated, type V, alpha subunit gene (SCN5A, 600163.0033);

Prefixed ID : #614022;

Details

Origin ID

614022;

UMLS CUI

C3151464;

DO Cross reference
- familial atrial fibrillation [DO Concept]
Genes related to phenotype
- Sodium voltage-gated channel, alpha subunit 5 [OMIM gene]
HPO term(s)
- Atrial flutter [HPO term]
- Autosomal dominant inheritance [HPO term]
- Left atrial enlargement [HPO term]
- Left ventricular hypertrophy [HPO term]
- Paroxysmal atrial fibrillation [HPO term]
- Paroxysmal atrial tachycardia [HPO term]
- Tricuspid regurgitation [HPO term]
ORDO concept(s)
- Familial atrial fibrillation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to NTBT
- Familial atrial fibrillation [ORDO Disease]
- familial atrial fibrillation [DO Concept]

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