ATFB2
MCID: ATR025
MIFTS: 13

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 58 13 74
Atfb2 58

Classifications:



External Ids:

OMIM 58 608988
MedGen 43 C1837812
UMLS 74 C1837812

Summaries for Atrial Fibrillation, Familial, 2

OMIM : 58 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 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
Content
Loading form....