Primary atrial arrhythmia

Symptom Information:

Symptom ID: HPO:0001692
Synonyms:
Atrial arrhythmia [HPO:0001692]
Atrial arrhythmia [OMIM:Atrial arrhythmia]
Quality:
Cross references:
OMIM: "Atrial arrhythmia" [OMIM:Atrial arrhythmia]
Is a (Direct Parents):
HPO         Supraventricular tachycardia
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)
                Tachycardia(HPO:0001649)
                   Supraventricular tachycardia(HPO:0004755)
                      Primary atrial arrhythmia(HPO:0001692)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

ATTRV122I amyloidosis (Orphanet:85451)
Atrial fibrillation, familial, 10 (OMIM:614022)
Autosomal dominant Emery-Dreifuss muscular dystrophy (Orphanet:98853)
Autosomal dominant limb-girdle muscular dystrophy type 1B (Orphanet:264)
Brugada syndrome (Orphanet:130)
Chronic atrial and intestinal dysrhythmia syndrome (Orphanet:435988)
Congenital heart block (Orphanet:60041)
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease (Orphanet:436242)
Familial long QT syndrome (Orphanet:768)
Long QT syndrome 1 (OMIM:192500)
Long QT syndrome 2 (OMIM:613688)
Long QT syndrome 3 (OMIM:603830)
Peripartum cardiomyopathy (Orphanet:563)
Romano-Ward syndrome (Orphanet:101016)
[DEL] CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY (OMIM:616117)
[DEL]EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED (OMIM:310300)