Amyloidosis

Symptom Information:

Symptom ID: HPO:0011034
Synonyms:
Amyloidosis, (Iowa type 107680.0010, nonneuropathic 107680.0016) [OMIM:Amyloidosis, (Iowa type 107680.0010, nonneuropathic 107680.0016)]
Amyloidosis [MedDRA:10002022]
Quality:
Cross references:
OMIM: "Amyloidosis, (Iowa type 107680.0010, nonneuropathic 107680.0016)" [OMIM:Amyloidosis, (Iowa type 107680.0010, nonneuropathic 107680.0016)]
Is a (Direct Parents):
MedDRA Amyloidoses
HPO         Abnormality of metabolism/homeostasis
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)
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)