Abnormal EKG

Symptom Information:

Symptom ID: HPO:0003115
Synonyms:
Abnormal EKG [OMIM:Abnormal EKG]
Quality:
Cross references:
OMIM: "Abnormal EKG" [OMIM:Abnormal EKG]
Is a (Direct Parents):
HPO         Abnormality of cardiovascular system physiology
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:
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)