Atrial fibrillation, familial, 1

Preferred Label : Atrial fibrillation, familial, 1;

Symbol : ATFB1;

CISMeF acronym : ATFB1;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Atrial fibrillation, autosomal dominant;

Description : Atrial fibrillation is the most common sustained cardiac rhythm disturbance, affecting more than 2 million Americans, with an overall prevalence of 0.89%. The prevalence increases rapidly with age, to 2.3% between the ages of 40 and 60 years, and to 5.9% over the age of 65. The most dreaded complication is thromboembolic stroke (Brugada et al., 1997). Beyer et al. (1993) suggested that a familial form of atrial fibrillation is rare. - Genetic Heterogeneity of Familial Atrial Fibrillation;

Inheritance : Autosomal dominant;

Prefixed ID : %608583;

Details

Origin ID

608583;

UMLS CUI

C1843687;

Broader ORDO disease(s)
- Familial atrial fibrillation [ORDO Disease]
Currated CISMeF NLP mapping
- atrial fibrillation, familial 1 [MeSH concept]
- atrial fibrillation, familial 1 [MeSH Supplementary Concept]
DO Cross reference
- familial atrial fibrillation [DO Concept]
HPO term(s)
- Atrial fibrillation [HPO term]
- Atrial fibrillation, isolated [HPO term]
- Autosomal dominant inheritance [HPO term]
- Heterogeneous [HPO term]
- Irregular heart beat [HPO term]
- Stroke [HPO term]
- Tachycardia [HPO term]
- Thromboembolic stroke [HPO term]
ORDO concept(s)
- Familial atrial fibrillation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- atrial fibrillation, familial 1 [MeSH Supplementary Concept]
- atrial fibrillation, familial 1 [MeSH concept]
Validated automatic mappings to NTBT
- Familial atrial fibrillation [ORDO Disease]
- familial atrial fibrillation [DO Concept]

Keyword's position in hierarchy(ies) :

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