Atrial fibrillation, familial, 9

Preferred Label : Atrial fibrillation, familial, 9;

Symbol : ATFB9;

CISMeF acronym : ATFB9;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the potassium channel, inwardly rectifying, subfamily J, member 2 gene (KCNJ1, 600681.0014);

Prefixed ID : #613980;

Details

Origin ID

613980;

UMLS CUI

C3151431;

DO Cross reference
- familial atrial fibrillation [DO Concept]
Genes related to phenotype
- Potassium channel, inwardly rectifying, subfamily j, member 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [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 [ORDO Disease]
- familial atrial fibrillation [DO Concept]

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