ATFB2
MCID: ATR025
MIFTS: 14

Atrial Fibrillation, Familial, 2 (ATFB2)

Categories: Blood diseases, Cardiovascular diseases, Genetic diseases, Rare diseases, Respiratory diseases

Aliases & Classifications for Atrial Fibrillation, Familial, 2

MalaCards integrated aliases for Atrial Fibrillation, Familial, 2:

Name: Atrial Fibrillation, Familial, 2 57 13 73
Atfb2 57

Classifications:



External Ids:

OMIM 57 608988
MedGen 42 C1837812
UMLS 73 C1837812

Summaries for Atrial Fibrillation, Familial, 2

OMIM : 57 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). For a discussion of genetic heterogeneity of atrial fibrillation, see 608583. (608988)

MalaCards based summary : Atrial Fibrillation, Familial, 2, also known as atfb2, is related to familial atrial fibrillation and atrial fibrillation. An important gene associated with Atrial Fibrillation, Familial, 2 is ATFB2 (Familial Atrial Fibrillation 2).

Related Diseases for Atrial Fibrillation, Familial, 2

Symptoms & Phenotypes for Atrial Fibrillation, Familial, 2

Clinical features from OMIM:

608988

Drugs & Therapeutics for Atrial Fibrillation, Familial, 2

Search Clinical Trials , NIH Clinical Center for Atrial Fibrillation, Familial, 2

Genetic Tests for Atrial Fibrillation, Familial, 2

Anatomical Context for Atrial Fibrillation, Familial, 2

Publications for Atrial Fibrillation, Familial, 2

Variations for Atrial Fibrillation, Familial, 2

Expression for Atrial Fibrillation, Familial, 2

Search GEO for disease gene expression data for Atrial Fibrillation, Familial, 2.

Pathways for Atrial Fibrillation, Familial, 2

GO Terms for Atrial Fibrillation, Familial, 2

Sources for Atrial Fibrillation, Familial, 2

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
Content
Loading form....