Atrial fibrillation, familial, 13

Preferred Label : Atrial fibrillation, familial, 13;

Symbol : ATFB13;

CISMeF acronym : ATFB13;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the sodium channel, voltage-gated, type I, beta polypeptide gene (SCN1B, 600235.0006);

Prefixed ID : #615377;

Details

Origin ID

615377;

UMLS CUI

C3809311;

DO Cross reference
- familial atrial fibrillation [DO Concept]
Genes related to phenotype
- Sodium voltage-gated channel, beta subunit 1 [OMIM gene]
HPO term(s)
- Aortic valve stenosis [HPO term]
- Autosomal dominant inheritance [HPO term]
- Left atrial enlargement [HPO term]
- Paroxysmal atrial fibrillation [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 [DO Concept]

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