Left ventricular failure
Symptom Information:
Symptom ID: | HPO:0005162 | ||
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) Abnormal heart morphology(HPO:0001627) obsolete Malformation of the heart and great vessels(HPO:0002564) Abnormality of cardiac ventricle(HPO:0001713) Abnormality of the left ventricle(HPO:0001711) Left ventricular failure(HPO:0005162) MedDRA: |
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Database Frequency: | 18 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction | (OMIM:612158) |
Cardiomyopathy, dilated, 1D | (OMIM:601494) |
Cardiomyopathy, dilated, 1EE | (OMIM:613252) |
Cardiomyopathy, familial hypertrophic, 7 | (OMIM:613690) |
Cardiomyopathy, familial restrictive, 3 | (OMIM:612422) |
Cirrhotic cardiomyopathy | (Orphanet:57777) |
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | (Orphanet:300751) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemochromatosis, type 2B | (OMIM:613313) |
His bundle tachycardia | (Orphanet:3283) |
Left ventricular noncompaction 8 | (OMIM:615373) |
MELAS | (Orphanet:550) |
Peripartum cardiomyopathy | (Orphanet:563) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Tako-Tsubo cardiomyopathy | (Orphanet:66529) |