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Parent Node:
expandkidney disease (MONDO:0005240)
..Starting node
..expandfamilial juvenile hyperuricemic nephropathy ()

       Child Nodes:
........expandfamilial juvenile hyperuricemic nephropathy type 1 ()
........expandfamilial juvenile hyperuricemic nephropathy type 2 ()
........expandhyperuricemic nephropathy, familial juvenile type 3 ()
........expandhyperuricemic nephropathy, familial juvenile type 4 ()



 Sister Nodes: 
..expandAlsing syndrome ()
..expandanuria ()
..expandArnold stickler bourne syndrome ()
..expandatheroembolism of kidney ()
..expandC1q nephropathy ()
..expandchronic kidney disease ()
..expandcongenital anomaly of kidney and urinary tract ()
..expandcrush syndrome ()
..expandcystic kidney disease ()
..expanddiabetes insipidus ()
..expandfamilial juvenile hyperuricemic nephropathy ()
..expandglomerular disease ()
..expandhantavirus hemorrhagic fever with renal syndrome ()
..expandhematological disorder with renal involvement ()
..expandhydronephrosis ()
..expandhypertensive renal disease ()
..expandimpaired renal function disease ()
..expandinherited renal cancer-predisposing syndrome ()
..expandkidney cortex necrosis ()
..expandkidney failure ()
..expandkidney hypertrophy ()
..expandkidney neoplasm ()
..expandkidney papillary necrosis ()
..expandlachiewicz sibley syndrome ()
..expandnephritis ()
..expandnephrocalcinosis ()
..expandnephrolithiasis ()
..expandnephropathy secondary to a storage or other metabolic disease ()
..expandnephropathy-associated ciliopathy ()
..expandnephrosis ()
..expandobstructive nephropathy ()
..expandorthostatic proteinuria ()
..expandperinephritis ()
..expandproteinuria ()
..expandpyonephrosis ()
..expandrare cause of hypertension ()
..expandrare renal tubular disease ()
..expandrenal aminoaciduria ()
..expandrenal artery disease ()
..expandrenal disease with cataract ()
..expandrenal hypertension ()
..expandrenal infectious disease ()
..expandrenal tuberculosis ()
..expandrenal tubule disease ()
..expandstricture or kinking of ureter ()
..expandthrombotic microangiopathy ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:608
Name:familial juvenile hyperuricemic nephropathy
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:familial juvenile gouty nephropathy; familial juvenile hyperuricemic nephropathy; familial nephropathy associated with hyperuricemia; familial nephropathy with gout; FJHN; gouty nephropathy, familial; gouty nephropathy, familial juvenile; juvenile gout; juvenile gouty nephropathy; nephropathy, famil
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
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