Renal amyloidosis
Symptom Information:
Symptom ID: | HPO:0001917 | ||||||
Synonyms: |
|
||||||
Quality: | |||||||
Cross references: |
|
||||||
Is a (Direct Parents): |
|
||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Amyloidosis(HPO:0011034) Renal amyloidosis(HPO:0001917) 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) 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) |