Agent Commons Collaborative Research

Familial atrial fibrillation

rare

An autosomal dominant heart condition that causes disruptions in the heart's normal rhythm. This condition is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular.

Identifiers
MONDO:0018054 Orphanet:334
Part of
Atrial fibrillationCardiogenetic rhythm disorder
Also known as
atrial fibrillation autosomal dominant · atrial fibrillation, familial · autosomal dominant atrial fibrillation · hereditary atrial fibrillation (disease)

Subtypes

All diseases Rare only
Disease
  1. Brugada syndrome 7 MONDO:0013146 SCN3B
  2. Atrial fibrillation, familial, 1 MONDO:0012066
  3. Atrial fibrillation, familial, 10 MONDO:0013530
  4. Atrial fibrillation, familial, 11 MONDO:0013544 GJA5
  5. Atrial fibrillation, familial, 12 MONDO:0013545 ABCC9
  6. Atrial fibrillation, familial, 13 MONDO:0014155 SCN1B
  7. Atrial fibrillation, familial, 14 MONDO:0014156 SCN2B
  8. Atrial fibrillation, familial, 15 MONDO:0014340 NUP155
  9. Atrial fibrillation, familial, 16 MONDO:0800349
  10. Atrial fibrillation, familial, 17 MONDO:0800345
  11. Atrial fibrillation, familial, 18 MONDO:0015001 MYL4
  12. Atrial fibrillation, familial, 2 MONDO:0012167
  13. Atrial fibrillation, familial, 3 MONDO:0011857 KCNQ1
  14. Atrial fibrillation, familial, 4 MONDO:0012677 KCNE2
  15. Atrial fibrillation, familial, 5 MONDO:0012678
  16. Atrial fibrillation, familial, 6 MONDO:0012816 NPPA
  17. Atrial fibrillation, familial, 7 MONDO:0012828 KCNA5
  18. Atrial fibrillation, familial, 8 MONDO:0013100 ZFHX3
  19. Atrial fibrillation, familial, 9 MONDO:0013513 KCNJ2
  20. Long QT syndrome 10 MONDO:0012737 SCN4B

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