EKG: T-wave inversion
Symptom Information:
| Symptom ID: | HPO:0010872 | ||
| 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) EKG: T-wave inversion(HPO:0010872) 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, 12 | (OMIM:611528) |
| Arrhythmogenic right ventricular dysplasia, familial, 2 | (OMIM:600996) |
| Arrhythmogenic right ventricular dysplasia, familial, 8 | (OMIM:607450) |
| Arrhythmogenic right ventricular dysplasia, familial, 9 | (OMIM:609040) |
| Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
| Cardiomyopathy, dilated, 1S | (OMIM:613426) |
| Cardiomyopathy, dilated, 1Z | (OMIM:611879) |
| Cardiomyopathy, familial hypertrophic, 12 | (OMIM:612124) |
| Cardiomyopathy, familial hypertrophic, 14 | (OMIM:613251) |
| Cardiomyopathy, familial restrictive 2 | (OMIM:609578) |
| Fabry disease | (Orphanet:324) |
| Familial isolated arrhythmogenic right ventricular dysplasia | (Orphanet:217656) |
| Friedreich ataxia 1 | (OMIM:229300) |
| Hypertrophic cardiomyopathy due to intensive athletic training | (Orphanet:217601) |
| Jervell and Lange-Nielsen syndrome | (Orphanet:90647) |
| Naxos disease | (Orphanet:34217) |
| Uhl anomaly | (Orphanet:3403) |