Paroxysmal atrial fibrillation
Symptom Information:
Symptom ID: | HPO:0004757 | ||||
Synonyms: |
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Is a (Direct Parents): |
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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) Supraventricular arrhythmia(HPO:0005115) Supraventricular tachycardia(HPO:0004755) Primary atrial arrhythmia(HPO:0001692) Atrial fibrillation(HPO:0005110) Paroxysmal atrial fibrillation(HPO:0004757) Tachycardia(HPO:0001649) Supraventricular tachycardia(HPO:0004755) Primary atrial arrhythmia(HPO:0001692) Atrial fibrillation(HPO:0005110) Paroxysmal atrial fibrillation(HPO:0004757) MedDRA: |
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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) |