Atrial fibrillation, familial, 18

Preferred Label : Atrial fibrillation, familial, 18;

Symbol : ATFB18;

CISMeF acronym : ATFB18;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the embryonic atrial alkali myosin light chain-4 gene (MYL4, 160770.0001);

Prefixed ID : #617280;

Details

Origin ID

617280;

UMLS CUI

C4310636;

Genes related to phenotype
- Myosin, light chain 4, alkali, atrial, embryonic [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bradycardia [HPO term]
- Palpitations [HPO term]
- Paroxysmal atrial fibrillation [HPO term]
- Permanent atrial fibrillation [HPO term]
ORDO concept(s)
- Familial atrial fibrillation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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