Abnormal echocardiogram

Symptom Information:

Symptom ID: HPO:0003116
Synonyms:
Abnormal echocardiography [HPO:0003116]
Abnormal echocardiogram [OMIM:Abnormal echocardiogram]
Echocardiogram abnormal [MedDRA:10061593]
Quality:
Cross references:
OMIM: "Abnormal echocardiogram" [OMIM:Abnormal echocardiogram]
Is a (Direct Parents):
HPO         Abnormality of cardiovascular system physiology
MedDRA Cardiac function diagnostic procedures
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)
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)