Atrial fibrillation, familial, 12

Preferred Label : Atrial fibrillation, familial, 12;

Symbol : ATFB12;

CISMeF acronym : ATFB12;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the ATP-binding cassette, subfamily C, member 9 gene (ABCC9, 601439.0003);

Prefixed ID : #614050;

Details

Origin ID

614050;

UMLS CUI

C3279695;

DO Cross reference
- familial atrial fibrillation [DO Concept]
Genes related to phenotype
- Atp-binding cassette, subfamily C, member 9 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Middle age onset [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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