Paroxysmal supraventricular tachycardia
Symptom Information:
Symptom ID: | HPO:0004763 | ||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |