EKG: T-wave abnormalities
Symptom Information:
| Symptom ID: | HPO:0005135 | ||
| Synonyms: |
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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) EKG: T-wave abnormalities(HPO:0005135) MedDRA: |
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| Database Frequency: | 19 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Arrhythmogenic right ventricular dysplasia, familial, 10 | (OMIM:610193) |
| Arrhythmogenic right ventricular dysplasia, familial, 11 | (OMIM:610476) |
| Arrhythmogenic right ventricular dysplasia, familial, 13 | (OMIM:615616) |
| Arrhythmogenic right ventricular dysplasia, familial, 8 | (OMIM:607450) |
| Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
| Cardiomyopathy, familial hypertrophic, 12 | (OMIM:612124) |
| Cardiomyopathy, familial hypertrophic, 19 | (OMIM:613875) |
| Cardiomyopathy, familial hypertrophic, 20 | (OMIM:613876) |
| Familial long QT syndrome | (Orphanet:768) |
| Familial short QT syndrome | (Orphanet:51083) |
| Hypertrophic cardiomyopathy due to intensive athletic training | (Orphanet:217601) |
| Long QT syndrome 1 | (OMIM:192500) |
| Long QT syndrome 10 | (OMIM:611819) |
| Long QT syndrome 2 | (OMIM:613688) |
| Long QT syndrome 3 | (OMIM:603830) |
| Naxos disease | (Orphanet:34217) |
| Rett syndrome | (Orphanet:778) |
| Romano-Ward syndrome | (Orphanet:101016) |
| Woodhouse-Sakati syndrome | (Orphanet:3464) |