Details of Disease

General Information of Disease (ID: DIS6ATU4)

Disease Name Familial juvenile hyperuricemic nephropathy
Synonyms
gouty nephropathy, familial; tubulointerstitial kidney disease; nephropathy, familial, with gout; juvenile gouty nephropathy; juvenile gout; gouty nephropathy, familial juvenile; familial nephropathy with gout; familial nephropathy associated with hyperuricemia; familial juvenile hyperuricemic nephropathy; familial juvenile gouty nephropathy; FJHN
Disease Hierarchy
DISNCQLA: Inherited kidney disorder
DIS6ATU4: Familial juvenile hyperuricemic nephropathy
Disease Identifiers
MONDO ID
MONDO_0000608
UMLS CUI
C0268113
MedGen ID
75651
SNOMED CT ID
46785007

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 2 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
SLC22A6 TTTYH7A Strong Genetic Variation [1]
SLC2A9 TTIF3GB Strong Biomarker [1]
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References

1 Urate transport via human PAH transporter hOAT1 and its gene structure. Kidney Int. 2003 Jan;63(1):143-55.