Generalized amyloid deposition
Symptom Information:
| Symptom ID: | HPO:0003216 | ||
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Amyloidosis(HPO:0011034) Generalized amyloid deposition(HPO:0003216) MedDRA: |
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| Database Frequency: | 4 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Autosomal dominant beta2-microglobulinic amyloidosis | (Orphanet:314652) |
| Familial amyloidosis, Finnish type | (Orphanet:85448) |
| Familial renal amyloidosis | (Orphanet:85450) |
| Hereditary cerebral hemorrhage with amyloidosis, Icelandic type | (Orphanet:100008) |