Reduced systolic function
Symptom Information:
Symptom ID: | HPO:0006673 | ||
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) Congestive heart failure(HPO:0001635) Reduced systolic function(HPO:0006673) MedDRA: |
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Database Frequency: | 11 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Cardiomyopathy, dilated, 1E | (OMIM:601154) |
Cardiomyopathy, dilated, 1FF | (OMIM:613286) |
Cardiomyopathy, dilated, 1I | (OMIM:604765) |
Cardiomyopathy, dilated, 1L | (OMIM:606685) |
Cardiomyopathy, dilated, 1P | (OMIM:609909) |
Cardiomyopathy, dilated, 1T | (OMIM:613740) |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | (OMIM:615821) |
Cirrhotic cardiomyopathy | (Orphanet:57777) |
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | (Orphanet:300751) |
Friedreich ataxia 1 | (OMIM:229300) |
Mulibrey nanism | (Orphanet:2576) |