Paroxysmal supraventricular tachycardia

Symptom Information:

Symptom ID: HPO:0004763
Synonyms:
Paroxysmal supraventricular tachycardia [OMIM:Paroxysmal supraventricular tachycardia]
Quality:
Cross references:
OMIM: "Paroxysmal supraventricular tachycardia" [OMIM:Paroxysmal supraventricular tachycardia]
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)
                      Paroxysmal supraventricular tachycardia(HPO:0004763)
                Tachycardia(HPO:0001649)
                   Supraventricular tachycardia(HPO:0004755)
                      Paroxysmal supraventricular tachycardia(HPO:0004763)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Atrial tachyarrhythmia with short PR interval (Orphanet:844)
Autosomal dominant limb-girdle muscular dystrophy type 1B (Orphanet:264)
Familial sick sinus syndrome (Orphanet:166282)
Hidrotic ectodermal dysplasia, Christianson-Fourie type (Orphanet:1808)
Severe achondroplasia - developmental delay - acanthosis nigricans (Orphanet:85165)
Spondyloepimetaphyseal dysplasia - hypotrichosis (Orphanet:168443)
Spondyloepimetaphyseal dysplasia, Geneviève type (Orphanet:168454)
THANATOPHORIC DYSPLASIA, TYPE II (OMIM:187601)
Thanatophoric dysplasia type 1 (Orphanet:1860)
WOLFF-PARKINSON-WHITE SYNDROME (OMIM:194200)