Abnormal echocardiogram
Symptom Information:
Symptom ID: | HPO:0003116 | ||||
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 echocardiogram(HPO:0003116) MedDRA: Investigations(MedDRA:10022891) Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512) Cardiac function diagnostic procedures(MedDRA:10007566) Abnormal echocardiogram(HPO:0003116) |
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Database Frequency: | 33 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
AA amyloidosis | (Orphanet:85445) |
AL amyloidosis | (Orphanet:85443) |
ATTRV122I amyloidosis | (Orphanet:85451) |
Alpha-mannosidosis | (Orphanet:61) |
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, 8 | (OMIM:607450) |
Arrhythmogenic right ventricular dysplasia, familial, 9 | (OMIM:609040) |
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
Cardiomyopathy, dilated, 1D | (OMIM:601494) |
Cardiomyopathy, familial hypertrophic, 12 | (OMIM:612124) |
Cardiomyopathy, familial hypertrophic, 13 | (OMIM:613243) |
Cardiomyopathy, familial hypertrophic, 14 | (OMIM:613251) |
Cardiomyopathy, familial hypertrophic, 15 | (OMIM:613255) |
Cardiomyopathy, familial hypertrophic, 17 | (OMIM:613873) |
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) |
FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA | (OMIM:229310) |
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
Friedreich ataxia 1 | (OMIM:229300) |
Friedreich ataxia 2 | (OMIM:601992) |
Hypertrophic cardiomyopathy due to intensive athletic training | (Orphanet:217601) |
Idiopathic recurrent pericarditis | (Orphanet:251307) |
MERRF | (Orphanet:551) |
Steinert myotonic dystrophy | (Orphanet:273) |