Prolonged QT interval
Symptom Information:
Symptom ID: | HPO:0001657 | |||||||||
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) Abnormal EKG(HPO:0003115) Prolonged QT interval(HPO:0001657) MedDRA: Cardiac disorders(MedDRA:10007541) Arrhythmia(HPO:0011675) Cardiac conduction disorders(MedDRA:10000032) Prolonged QT interval(HPO:0001657) Investigations(MedDRA:10022891) Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512) ECG investigations(MedDRA:10053104) Arrhythmia(HPO:0011675) Cardiac conduction disorders(MedDRA:10000032) Prolonged QT interval(HPO:0001657) Heart rate and pulse investigations(MedDRA:10053103) Arrhythmia(HPO:0011675) Cardiac conduction disorders(MedDRA:10000032) Prolonged QT interval(HPO:0001657) |
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Database Frequency: | 33 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Atrial fibrillation, familial, 10 | (OMIM:614022) |
Atrial fibrillation, familial, 17 | (ORPHA:334) |
Atrial fibrillation, familial, 3 | (OMIM:607554) |
Atrial fibrillation, familial, 7 | (OMIM:612240) |
Brugada syndrome | (Orphanet:130) |
Cardiac arrhythmia, ankyrin-B-related | (OMIM:600919) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cardiomyopathy, familial hypertrophic, 13 | (OMIM:613243) |
Cirrhotic cardiomyopathy | (Orphanet:57777) |
Dilated cardiomyopathy with ataxia | (Orphanet:66634) |
Familial long QT syndrome | (Orphanet:768) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Glycogen storage disease due to muscle and heart glycogen synthase deficiency | (Orphanet:137625) |
Jervell and Lange-Nielsen syndrome | (Orphanet:90647) |
Jervell and Lange-Nielsen syndrome 1 | (OMIM:220400) |
Jervell and Lange-Nielsen syndrome 2 | (OMIM:612347) |
Long QT syndrome 1 | (OMIM:192500) |
Long QT syndrome 10 | (OMIM:611819) |
Long QT syndrome 11 | (OMIM:611820) |
Long QT syndrome 13 | (OMIM:613485) |
Long QT syndrome 2 | (OMIM:613688) |
Long QT syndrome 3 | (OMIM:603830) |
Long QT syndrome 5 | (OMIM:613695) |
Long QT syndrome 6 | (OMIM:613693) |
Long QT syndrome 9 | (OMIM:611818) |
MELAS | (Orphanet:550) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14 | (OMIM:615351) |
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | (OMIM:604559) |
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome | (Orphanet:228012) |
Romano-Ward syndrome | (Orphanet:101016) |
Sick sinus syndrome 1, autosomal recessive | (OMIM:608567) |
Timothy syndrome | (Orphanet:65283) |
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 | (OMIM:107970) |