Supraventricular tachycardia

Symptom Information:

Symptom ID: HPO:0004755
Synonyms:
Supraventricular tachyarrhythmia [HPO:0004755]
Supraventricular tachyarrhythmias [OMIM:Supraventricular tachyarrhythmias]
Supraventricular tachycardia (SVtach) [OMIM:Supraventricular tachycardia (SVtach)]
Supraventricular tachyarrhythmia [MedDRA:10065342]
Supraventricular tachycardia [MedDRA:10042604]
Quality:
Cross references:
OMIM: "Supraventricular tachyarrhythmias" [OMIM:Supraventricular tachyarrhythmias]
OMIM: "Supraventricular tachycardia (SVtach)" [OMIM:Supraventricular tachycardia (SVtach)]
Is a (Direct Parents):
HPO         Tachycardia
HPO         Supraventricular 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)
                Supraventricular arrhythmia(HPO:0005115)
                   Supraventricular tachycardia(HPO:0004755)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Arrhythmia(HPO:0011675)
       Supraventricular arrhythmia(HPO:0005115)
          Supraventricular tachycardia(HPO:0004755)
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)
                Supraventricular tachycardia(HPO:0004755)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Supraventricular arrhythmia(HPO:0005115)
                Supraventricular tachycardia(HPO:0004755)
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

Atrial fibrillation, familial, 10 (OMIM:614022)
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction (OMIM:612158)
Cardiomyopathy, dilated, 1DD (OMIM:613172)
Cardiomyopathy, dilated, 1E (OMIM:601154)
Cardiomyopathy, dilated, 1EE (OMIM:613252)
Cardiomyopathy, familial hypertrophic, 2 (OMIM:115195)
Cardiomyopathy, familial restrictive, 3 (OMIM:612422)
Catecholaminergic polymorphic ventricular tachycardia (Orphanet:3286)
Fabry disease (Orphanet:324)
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease (Orphanet:436242)
Hemochromatosis, type 2A (OMIM:602390)
Histiocytoid cardiomyopathy (Orphanet:137675)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Incessant infant ventricular tachycardia (Orphanet:45453)
MERRF (Orphanet:551)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Multifocal atrial tachycardia (Orphanet:3282)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
Pyruvate dehydrogenase E3-binding protein deficiency (Orphanet:255182)
Uhl anomaly (Orphanet:3403)