WA 0821 7001 0763 (FORTRESS) Pintu Rumah Urat Kayu Nabunage Tolikara

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HPRT1
- Hyperuricemia
- Gout
- Acute Uric Acid Nephropathy
- Hypoxanthine Guanine Phosphoribosyltransferase Partial Deficiency
- Lesch–nyhan Syndrome
SLC2A9
- Renal Hypouricemia
- Gout
- Hyperuricemia
- Gout
- Lesch–nyhan Syndrome
ABCG2
- Hyperuricemia
- Uric Acid Concentration, Serum, Quantitative Trait Locus 1
- Gout
- Lesch–nyhan Syndrome
SLC22A12
- Renal Hypouricemia
- Hyperuricemia
- Gout
- Acute Uric Acid Nephropathy
- Lesch–nyhan Syndrome
UMOD
- Hyperuricemia
- Gout
- Autosomal Dominant Tubulointerstitial Kidney Disease, Umod-Related
- Hyperuricemic Nephropathy, Familial Juvenile, 2
PRPS1
- Phosphoribosylpyrophosphate Synthetase Superactivity
- Hyperuricemia
- Gout
- Acute Uric Acid Nephropathy
G6PC
- Hyperuricemia
- Gout
- Glycogen Storage Disease Type I
HNF1B
- Hyperuricemia
- Gout
- Autosomal Dominant Tubulointerstitial Kidney Disease, Umod-Related
- Fanconi Renotubular Syndrome 4 With Maturity-Onset Diabetes Of The Young
XDH
- Hyperuricemia
- Gout
- Lesch–nyhan Syndrome
ALDH16A1
- Hyperuricemia
- Gout
- Hypoxanthine Guanine Phosphoribosyltransferase Partial Deficiency
TTPA
- Familial Isolated Vitamin E Deficiency
REN
- Hyperuricemia
- Hyperuricemic Nephropathy, Familial Juvenile, 2
FMR1
- Renpenning's Syndrome
- Fragile X-Associated Tremor/ataxia Syndrome
SLC37A4
- Hyperuricemia
- Gout
- Glycogen Storage Disease Type I
PQBP1
- Renpenning's Syndrome
FAM20A
- Enamel-Renal Syndrome
IFIH1
- Singleton Merten Syndrome
SLC17A3
- Hyperuricemia
- Gout
- Uric Acid Concentration, Serum, Quantitative Trait Locus 4
ASS1
- Citrullinemia Type I
UOX
- Hyperuricemia
- Tumor Lysis Syndrome