Amyloidosis
Symptom Information:
Symptom ID: | HPO:0011034 | ||||
Synonyms: |
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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 metabolism/homeostasis(HPO:0001939) Amyloidosis(HPO:0011034) MedDRA: Immune system disorders(MedDRA:10021428) Immune disorders NEC(MedDRA:10027665) Amyloidoses(MedDRA:10002023) Amyloidosis(HPO:0011034) |
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Database Frequency: | 12 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
AA amyloidosis | (Orphanet:85445) |
AL amyloidosis | (Orphanet:85443) |
AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION | (OMIM:204850) |
AMYLOIDOSIS, CUTANEOUS BULLOUS | (OMIM:204900) |
Familial amyloid polyneuropathy | (Orphanet:85447) |
Familial primary localized cutaneous amyloidosis | (Orphanet:353220) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary localized amyloidosis | (Orphanet:314709) |
Primary systemic amyloidosis | (Orphanet:314701) |
Senile systemic amyloidosis | (Orphanet:330001) |
TRAPS syndrome | (Orphanet:32960) |
X-linked reticulate pigmentary disorder with systemic manifestations | (Orphanet:85453) |