Atrial flutter

Symptom Information:

Symptom ID: HPO:0004749
Synonyms:
Atrial flutter [OMIM:Atrial flutter]
Atrial flutter (rare) [OMIM:Atrial flutter (rare)]
Atrial flutter [MedDRA:10003662]
Quality:
Cross references:
OMIM: "Atrial flutter" [OMIM:Atrial flutter]
OMIM: "Atrial flutter (rare)" [OMIM:Atrial flutter (rare)]
Is a (Direct Parents):
MedDRA Supraventricular arrhythmia
HPO         Primary atrial 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)
                Supraventricular arrhythmia(HPO:0005115)
                   Supraventricular tachycardia(HPO:0004755)
                      Primary atrial arrhythmia(HPO:0001692)
                         Atrial flutter(HPO:0004749)
                Tachycardia(HPO:0001649)
                   Supraventricular tachycardia(HPO:0004755)
                      Primary atrial arrhythmia(HPO:0001692)
                         Atrial flutter(HPO:0004749)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Arrhythmia(HPO:0011675)
       Supraventricular arrhythmia(HPO:0005115)
          Atrial flutter(HPO:0004749)
Investigations(MedDRA:10022891)
    Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Supraventricular arrhythmia(HPO:0005115)
                Atrial flutter(HPO:0004749)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Supraventricular arrhythmia(HPO:0005115)
                Atrial flutter(HPO:0004749)
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15 (OMIM:615770)
Atrial fibrillation, familial, 10 (OMIM:614022)
Atrial tachyarrhythmia with short PR interval (Orphanet:844)
BRUGADA SYNDROME 7 (OMIM:613120)
Brugada syndrome (Orphanet:130)
Cardiomyopathy, dilated, 1E (OMIM:601154)
Cardiomyopathy, familial restrictive 2 (OMIM:609578)
Chronic atrial and intestinal dysrhythmia syndrome (Orphanet:435988)
Familial atrial fibrillation (Orphanet:334)
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease (Orphanet:436242)
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation (Orphanet:300751)
Familial progressive cardiac conduction defect (Orphanet:871)
Familial sick sinus syndrome (Orphanet:166282)
Idiopathic neonatal atrial flutter (Orphanet:45452)
Lymphedema - atrial septal defects - facial changes (Orphanet:86915)
Senile systemic amyloidosis (Orphanet:330001)
Sinus node disease and myopia (OMIM:182190)
Steinert myotonic dystrophy (Orphanet:273)
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome (Orphanet:324410)
[DEL] CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY (OMIM:616117)