Renal amyloidosis

Symptom Information:

Symptom ID: HPO:0001917
Synonyms:
Renal amyloidosis [OMIM:Renal amyloidosis]
Renal amyloidosis (Iowa type 107680.0010, systemic nonneuronopathic 107680.0016) [OMIM:Renal amyloidosis (Iowa type 107680.0010, systemic nonneuronopathic 107680.0016)]
Renal amyloidosis [MedDRA:10038357]
Quality:
Cross references:
OMIM: "Renal amyloidosis" [OMIM:Renal amyloidosis]
OMIM: "Renal amyloidosis (Iowa type 107680.0010, systemic nonneuronopathic 107680.0016)" [OMIM:Renal amyloidosis (Iowa type 107680.0010, systemic nonneuronopathic 107680.0016)]
Is a (Direct Parents):
HPO         Amyloidosis
MedDRA Nephropathies and tubular disorders NEC
HPO         Abnormal renal morphology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal morphology(HPO:0012210)
                      Renal amyloidosis(HPO:0001917)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Amyloidosis(HPO:0011034)
             Renal amyloidosis(HPO:0001917)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Nephropathies and tubular disorders NEC(MedDRA:10029150)
          Renal amyloidosis(HPO:0001917)
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

AA amyloidosis (Orphanet:85445)
APOLIPOPROTEIN A-I (OMIM:107680)
FAMILIAL MEDITERRANEAN FEVER (OMIM:249100)
FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT (OMIM:134610)
Familial Mediterranean fever (Orphanet:342)
Familial cold urticaria (Orphanet:47045)
Muckle-Wells syndrome (Orphanet:575)
Polyarteritis nodosa, childhood-onset (OMIM:615688)