Familial juvenile hyperuricemic nephropathy type 1

Disease Export to PDF
Name:
Familial juvenile hyperuricemic nephropathy type 1
Description:
Familial juvenile hyperuricemic nephropathy type 1 (FJHN1) is a rare kidney disorder characterized by hyperuricemia, progressive nephropathy, and gout occurring at an early age.
ORPHAcode:
209886
Synonyms:
FJHN type 1
Familial juvenile gouty nephropathy
Familial nephropathy with gout
UMOD-associated FJHN
UMOD-associated familial juvenile hyperuricemic nephropathy
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
01 May 2019 - 11:58