Paroxysmal atrial fibrillation

Symptom Information:

Symptom ID: HPO:0004757
Synonyms:
ATRIAL FIBRILLATION, PAROXYSMAL [HPO:0004757]
Atrial fibrillation, paroxysmal [OMIM:Atrial fibrillation, paroxysmal]
Paroxysmal atrial fibrillation [OMIM:Paroxysmal atrial fibrillation]
Fibrillation, paroxysmal atrial [OMIM:Fibrillation, paroxysmal atrial]
Quality:
Cross references:
OMIM: "Atrial fibrillation, paroxysmal" [OMIM:Atrial fibrillation, paroxysmal]
OMIM: "Paroxysmal atrial fibrillation" [OMIM:Paroxysmal atrial fibrillation]
OMIM: "Fibrillation, paroxysmal atrial" [OMIM:Fibrillation, paroxysmal atrial]
Is a (Direct Parents):
HPO         Atrial fibrillation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of cardiovascular system physiology(HPO:0011025)
             Arrhythmia(HPO:0011675)
                Tachycardia(HPO:0001649)
                   Supraventricular tachycardia(HPO:0004755)
                      Primary atrial arrhythmia(HPO:0001692)
                         Atrial fibrillation(HPO:0005110)
                            Paroxysmal atrial fibrillation(HPO:0004757)
                Supraventricular arrhythmia(HPO:0005115)
                   Supraventricular tachycardia(HPO:0004755)
                      Primary atrial arrhythmia(HPO:0001692)
                         Atrial fibrillation(HPO:0005110)
                            Paroxysmal atrial fibrillation(HPO:0004757)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

ATRIAL FIBRILLATION, FAMILIAL, 14; ATFB14 (OMIM:615378)
Atrial fibrillation, familial, 10 (OMIM:614022)
Atrial fibrillation, familial, 11 (OMIM:614049)
Atrial fibrillation, familial, 12 (OMIM:614050)
Atrial fibrillation, familial, 17 (ORPHA:334)
Atrial fibrillation, familial, 3 (OMIM:607554)
Atrial fibrillation, familial, 7 (OMIM:612240)
Atrial fibrillation, familial, 9 (OMIM:613980)
Atrial tachyarrhythmia with short PR interval (Orphanet:844)
Cardiomyopathy, familial hypertrophic, 12 (OMIM:612124)
Catecholaminergic polymorphic ventricular tachycardia (Orphanet:3286)
Familial atrial fibrillation (Orphanet:334)
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease (Orphanet:436242)
Familial short QT syndrome (Orphanet:51083)
Familial sick sinus syndrome (Orphanet:166282)
WOLFF-PARKINSON-WHITE SYNDROME (OMIM:194200)