ATFB14
MCID: ATR068
MIFTS: 21
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Atrial Fibrillation, Familial, 14 (ATFB14)
Categories:
Blood diseases, Cardiovascular diseases, Genetic diseases, Rare diseases, Respiratory diseases
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MalaCards integrated aliases for Atrial Fibrillation, Familial, 14:
Characteristics:OMIM:56
Inheritance:
autosomal dominant
Miscellaneous:
saddle-back st-segment elevation shows beat-to-beat and day-to-day variability HPO:31Classifications:
MalaCards categories:
Global: Genetic diseases Rare diseases Anatomical: Blood diseases Cardiovascular diseases Respiratory diseases |
OMIM :
56
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 familial atrial fibrillation, see ATFB1 (608583). (615378)
MalaCards based summary : Atrial Fibrillation, Familial, 14, is also known as atfb14. An important gene associated with Atrial Fibrillation, Familial, 14 is SCN2B (Sodium Voltage-Gated Channel Beta Subunit 2). Affiliated tissues include heart, and related phenotypes are hypertension and paroxysmal atrial fibrillation UniProtKB/Swiss-Prot : 73 Atrial fibrillation, familial, 14: A familial form of atrial fibrillation, a common sustained cardiac rhythm disturbance. Atrial fibrillation is characterized by disorganized atrial electrical activity and ineffective atrial contraction promoting blood stasis in the atria and reduces ventricular filling. It can result in palpitations, syncope, thromboembolic stroke, and congestive heart failure. |
Human phenotypes related to Atrial Fibrillation, Familial, 14:31
Symptoms via clinical synopsis from OMIM:56Clinical features from OMIM:615378 |
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MalaCards organs/tissues related to Atrial Fibrillation, Familial, 14:40
Heart
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Articles related to Atrial Fibrillation, Familial, 14:
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ClinVar genetic disease variations for Atrial Fibrillation, Familial, 14:6 (show all 22)
UniProtKB/Swiss-Prot genetic disease variations for Atrial Fibrillation, Familial, 14:73
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Search
GEO
for disease gene expression data for Atrial Fibrillation, Familial, 14.
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