Abnormal EKG
Symptom Information:
Symptom ID: | HPO:0003115 | ||
Synonyms: |
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Quality: | |||
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) MedDRA: |
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Database Frequency: | 44 / 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, 13 | (OMIM:615616) |
Arrhythmogenic right ventricular dysplasia, familial, 2 | (OMIM:600996) |
Arrhythmogenic right ventricular dysplasia, familial, 5 | (OMIM:604400) |
Arrhythmogenic right ventricular dysplasia, familial, 8 | (OMIM:607450) |
Arrhythmogenic right ventricular dysplasia, familial, 9 | (OMIM:609040) |
Atrial standstill | (Orphanet:1344) |
Atrial standstill 1 | (OMIM:108770) |
Atrial standstill 2 | (OMIM:615745) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Brugada syndrome | (Orphanet:130) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
Cardiomyopathy, dilated, 1L | (OMIM:606685) |
Cardiomyopathy, dilated, 1V | (OMIM:613697) |
Cardiomyopathy, dilated, 3B | (OMIM:302045) |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | (OMIM:615821) |
Cardiomyopathy, familial hypertrophic, 1 | (OMIM:192600) |
Cardiomyopathy, familial hypertrophic, 13 | (OMIM:613243) |
Cardiomyopathy, familial hypertrophic, 14 | (OMIM:613251) |
Cardiomyopathy, familial hypertrophic, 17 | (OMIM:613873) |
Cardiomyopathy, familial hypertrophic, 18 | (OMIM:613874) |
Cardiomyopathy, familial hypertrophic, 19 | (OMIM:613875) |
Cardiomyopathy, familial hypertrophic, 2 | (OMIM:115195) |
Cardiomyopathy, familial hypertrophic, 20 | (OMIM:613876) |
Cardiomyopathy, familial hypertrophic, 21 | (OMIM:614676) |
Cardiomyopathy, familial hypertrophic, 3 | (OMIM:115196) |
Cardiomyopathy, familial hypertrophic, 4 | (OMIM:115197) |
Cardiomyopathy, familial hypertrophic, 7 | (OMIM:613690) |
Cardiomyopathy, familial hypertrophic, 9 | (OMIM:613765) |
Cardiomyopathy, hypertrophic, 25 | (OMIM:607487) |
FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA | (OMIM:229310) |
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | (Orphanet:300751) |
Friedreich ataxia 1 | (OMIM:229300) |
Friedreich ataxia 2 | (OMIM:601992) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
MUSCULAR DYSTROPHY, CARDIAC TYPE | (OMIM:309930) |
Marden-Walker syndrome | (Orphanet:2461) |
Nathalie syndrome | (Orphanet:2663) |
PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHICABNORMALITIES | (OMIM:178650) |
Peripartum cardiomyopathy | (Orphanet:563) |
Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome | (Orphanet:65282) |