Atrial fibrillation

Symptom Information:

Symptom ID: HPO:0005110
Synonyms:
Atrial fibrillation [OMIM:Atrial fibrillation]
Atrial fibrillation (in some patients) [OMIM:Atrial fibrillation (in some patients)]
Atrial fibrillation [MedDRA:10003658]
Quality:
Cross references:
OMIM: "Atrial fibrillation" [OMIM:Atrial fibrillation]
OMIM: "Atrial fibrillation (in some patients)" [OMIM:Atrial fibrillation (in some patients)]
Is a (Direct Parents):
HPO         Primary atrial arrhythmia
MedDRA Supraventricular arrhythmia
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)
                Supraventricular arrhythmia(HPO:0005115)
                   Supraventricular tachycardia(HPO:0004755)
                      Primary atrial arrhythmia(HPO:0001692)
                         Atrial fibrillation(HPO:0005110)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Arrhythmia(HPO:0011675)
       Supraventricular arrhythmia(HPO:0005115)
          Atrial fibrillation(HPO:0005110)
Investigations(MedDRA:10022891)
    Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Supraventricular arrhythmia(HPO:0005115)
                Atrial fibrillation(HPO:0005110)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Supraventricular arrhythmia(HPO:0005115)
                Atrial fibrillation(HPO:0005110)
Database Frequency: 71 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
AORTIC ANEURYSM, FAMILIAL THORACIC 9 (OMIM:616166)
ATRIAL FIBRILLATION, FAMILIAL, 1 (OMIM:608583)
ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15 (OMIM:615770)
ATRIAL FIBRILLATION, FAMILIAL, 4 (OMIM:611493)
ATRIAL FIBRILLATION, FAMILIAL, 6 (OMIM:612201)
ATRIAL SEPTAL DEFECT 6 (OMIM:613087)
ATTRV122I amyloidosis (Orphanet:85451)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Arrhythmogenic right ventricular dysplasia, familial, 3 (OMIM:602086)
Atrial fibrillation, familial, 11 (OMIM:614049)
Atrial fibrillation, familial, 3 (OMIM:607554)
Atrial septal defect - atrioventricular conduction defects syndrome (Orphanet:1479)
Autosomal recessive Emery-Dreifuss muscular dystrophy (Orphanet:98855)
BRUGADA SYNDROME 3 (OMIM:611875)
BRUGADA SYNDROME 4 (OMIM:611876)
Brugada syndrome (Orphanet:130)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 (OMIM:617047)
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3 (OMIM:614954)
Cardiac arrhythmia, ankyrin-B-related (OMIM:600919)
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction (OMIM:612158)
Cardiomyopathy, dilated, 1BB (OMIM:612877)
Cardiomyopathy, dilated, 1D (OMIM:601494)
Cardiomyopathy, dilated, 1DD (OMIM:613172)
Cardiomyopathy, dilated, 1E (OMIM:601154)
Cardiomyopathy, dilated, 1HH (OMIM:613881)
Cardiomyopathy, dilated, 1KK (OMIM:615248)
Cardiomyopathy, dilated, 1R (OMIM:613424)
Cardiomyopathy, dilated, 1S (OMIM:613426)
Cardiomyopathy, dilated, 2B (OMIM:614672)
Cardiomyopathy, familial hypertrophic, 16 (OMIM:613838)
Cardiomyopathy, familial hypertrophic, 18 (OMIM:613874)
Cardiomyopathy, familial hypertrophic, 20 (OMIM:613876)
Cardiomyopathy, familial hypertrophic, 3 (OMIM:115196)
Cardiomyopathy, familial hypertrophic, 6 (OMIM:600858)
Cardiomyopathy, familial hypertrophic, 7 (OMIM:613690)
Cardiomyopathy, familial restrictive 2 (OMIM:609578)
Cardiomyopathy, familial restrictive, 3 (OMIM:612422)
Catecholaminergic polymorphic ventricular tachycardia (Orphanet:3286)
Chronic atrial and intestinal dysrhythmia syndrome (Orphanet:435988)
Costello syndrome (Orphanet:3071)
Desminopathy (Orphanet:98909)
EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT (OMIM:614302)
Ebstein malformation (Orphanet:1880)
Fabry disease (Orphanet:324)
Familial atrial fibrillation (Orphanet:334)
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease (Orphanet:436242)
Familial cutaneous collagenoma (Orphanet:53296)
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation (Orphanet:300751)
Familial isolated hypertrophic cardiomyopathy (Orphanet:155)
Familial isolated restrictive cardiomyopathy (Orphanet:75249)
Friedreich ataxia 1 (OMIM:229300)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Hemochromatosis, type 2A (OMIM:602390)
Hypertaurinuric cardiomyopathy (OMIM:145350)
Idiopathic giant cell myocarditis (Orphanet:329874)
Left ventricular noncompaction (Orphanet:54260)
Left ventricular noncompaction 1 (OMIM:604169)
Loeffler endocarditis (Orphanet:75566)
Long QT syndrome 13 (OMIM:613485)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
SHORT QT SYNDROME 2 (OMIM:609621)
Senile systemic amyloidosis (Orphanet:330001)
Sick sinus syndrome 2, autosomal dominant (OMIM:163800)
Sinus node disease and myopia (OMIM:182190)
Steinert myotonic dystrophy (Orphanet:273)
Tropical endomyocardial fibrosis (Orphanet:75565)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH ORWITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY (OMIM:604772)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome (Orphanet:324410)
[DEL] CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY (OMIM:616117)