Peripheral edema
Symptom Information:
| Symptom ID: | HPO:0012398 | ||
| Synonyms: |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of fluid regulation(HPO:0011032) Edema(HPO:0000969) Peripheral edema(HPO:0012398) MedDRA: |
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| Database Frequency: | 12 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| ATTRV122I amyloidosis | (Orphanet:85451) |
| Familial isolated restrictive cardiomyopathy | (Orphanet:75249) |
| Hurler-Scheie syndrome | (Orphanet:93476) |
| Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
| Idiopathic giant cell myocarditis | (Orphanet:329874) |
| Idiopathic pulmonary fibrosis | (Orphanet:2032) |
| Lymphoid interstitial pneumonia | (Orphanet:79128) |
| Mulibrey nanism | (Orphanet:2576) |
| PEHO syndrome | (Orphanet:2836) |
| PEHO-like syndrome | (Orphanet:99807) |
| Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
| Uhl anomaly | (Orphanet:3403) |