Atrial fibrillation, familial, 11

Preferred Label : Atrial fibrillation, familial, 11;

Symbol : ATFB11;

CISMeF acronym : ATFB11;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the alpha-5 gap junction protein gene (GJA5, 121013.0001);

Prefixed ID : #614049;

Details

Origin ID

614049;

UMLS CUI

C3279693;

DO Cross reference
- familial atrial fibrillation [DO Concept]
Genes related to phenotype
- Gap junction protein, alpha-5 [OMIM gene]
HPO term(s)
- Atrial fibrillation [HPO term]
- Autosomal dominant inheritance [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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