Atrial fibrillation, familial, 6

Preferred Label : Atrial fibrillation, familial, 6;

Symbol : ATFB6;

CISMeF acronym : ATFB6;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the natriuretic peptide precursor A gene (NPPA, 108780.0001);

Prefixed ID : #612201;

Details

Origin ID

612201;

UMLS CUI

C2677294;

Broader ORDO disease(s)
- Familial atrial fibrillation [ORDO Disease]
Currated CISMeF NLP mapping
- atrial fibrillation, familial, 6 [MeSH concept]
- atrial fibrillation, familial, 6 [MeSH Supplementary Concept]
DO Cross reference
- familial atrial fibrillation [DO Concept]
Genes related to phenotype
- Natriuretic peptide precursor a [OMIM gene]
HPO term(s)
- Atrial fibrillation [HPO term]
- Autosomal dominant inheritance [HPO term]
ORDO concept(s)
- Familial atrial fibrillation [ORDO Disease]
See also inter- (CISMeF)
- Familial atrial fibrillation [ORDO Disease]
- NPPA wt Allele [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- atrial fibrillation, familial, 6 [MeSH Supplementary Concept]
- atrial fibrillation, familial, 6 [MeSH concept]
Validated automatic mappings to NTBT
- familial atrial fibrillation [DO Concept]

Keyword's position in hierarchy(ies) :

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