Diastolic dysfunction
Symptom Information:
| Symptom ID: | MedDRA:10052337 | ||
| Synonyms: |
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| Is a (Whole tree): |
HPO:
MedDRA: Cardiac disorders(MedDRA:10007541) Abnormality of the myocardium(HPO:0001637) Myocardial disorders NEC(MedDRA:10028590) Diastolic dysfunction(MedDRA:10052337) |
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| Database Frequency: | 14 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| AL amyloidosis | (Orphanet:85443) |
| CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 | (OMIM:617047) |
| Cardiomyopathy, familial hypertrophic, 13 | (OMIM:613243) |
| Cardiomyopathy, familial hypertrophic, 16 | (OMIM:613838) |
| Cirrhotic cardiomyopathy | (Orphanet:57777) |
| Fabry disease | (Orphanet:324) |
| Familial isolated hypertrophic cardiomyopathy | (Orphanet:155) |
| Friedreich ataxia 1 | (OMIM:229300) |
| Hypertrophic cardiomyopathy due to intensive athletic training | (Orphanet:217601) |
| Left ventricular noncompaction | (Orphanet:54260) |
| Left ventricular noncompaction 1 | (OMIM:604169) |
| Left ventricular noncompaction 8 | (OMIM:615373) |
| Primary hyperoxaluria type 1 | (Orphanet:93598) |
| Primary systemic amyloidosis | (Orphanet:314701) |