{"context":{"query":"HYPOURICEMIA,HYPERURICEMIA"},"stats":{"total":50},"pagination":{"has_next":true,"next_token":"1,0,-1,38"},"schema":"id|dataset|name|xref_count","data":["C537757|mesh|Renal hypouricemia|164","C564405|mesh|Hypouricemia, Familial Renal, due to Tubular Hypersecretion|1","C565475|mesh|Hypouricemia, Hypercalcinuria, and Decreased Bone Density|1","C567426|mesh|Hypouricemia, Renal, 2|102","MONDO:0009071|mondo|hereditary renal hypouricemia|14","MONDO:0009438|mondo|hypouricemia, hypercalcinuria, and decreased bone density|3","MONDO:0010620|mondo|hypouricemia, familial renal, due to tubular hypersecretion|3","MONDO:0012793|mondo|hypouricemia, renal, 2|396","MONDO:0020728|mondo|hypouricemia, renal 1|186","MONDO:0968951|mondo|hypouricemia, renal|6","HP:0003537|hpo|Hypouricemia|73","94088|orphanet|Hereditary renal hypouricemia|28","C535995|mesh|Deafness hyperuricemia neurologic ataxia|1","C536137|mesh|Medullary cystic kidney disease 1|186","C537696|mesh|Juvenile gout|1","C537897|mesh|Phosphoribosylpyrophosphate synthetase deficiency|1","C562583|mesh|Gout, HPRT-Related|299","C563693|mesh|Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria|1","C565489|mesh|Hyperuricemia, Infantile, with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltransferase|1","C567760|mesh|Hyperuricemic Nephropathy, Familial Juvenile 2|217","D007926|mesh|Lesch-Nyhan Syndrome|271","D033461|mesh|Hyperuricemia|1768","EFO:0009104|efo|hyperuricemia|931","MONDO:0000608|mondo|familial juvenile hyperuricemic nephropathy|467","MONDO:0008073|mondo|familial juvenile hyperuricemic nephropathy type 1|759","MONDO:0008264|mondo|autosomal dominant medullary cystic kidney disease with or without hyperuricemia|178","MONDO:0009408|mondo|hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase|361","MONDO:0010298|mondo|Lesch-Nyhan syndrome|398","MONDO:0010299|mondo|hypoxanthine guanine phosphoribosyltransferase partial deficiency|564","MONDO:0013128|mondo|familial juvenile hyperuricemic nephropathy type 2|332","MONDO:0013458|mondo|hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome|4920","MONDO:0020726|mondo|tubulointerstitial kidney disease, autosomal dominant, 2|192","MONDO:0043176|mondo|phosphoribosylpyrophosphate synthetase deficiency|162","HP:0002149|hpo|Hyperuricemia|160","209886|orphanet|OBSOLETE: Familial juvenile hyperuricemic nephropathy type 1|307","217330|orphanet|REN-related autosomal dominant tubulointerstitial kidney disease|101","34149|orphanet|Autosomal dominant tubulointerstitial kidney disease|343","363694|orphanet|Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome|173","510|orphanet|Lesch-Nyhan syndrome|239","79233|orphanet|Hypoxanthine guanine phosphoribosyltransferase partial deficiency|204","88949|orphanet|MUC1-related autosomal dominant tubulointerstitial kidney disease|30","88950|orphanet|UMOD-related autosomal dominant tubulointerstitial kidney disease|311","GCST004825|gwas_study||3","GCST005801|gwas_study||18","GCST005802|gwas_study||2","GCST007916|gwas_study||24","GCST008460|gwas_study||28","GCST90129647|gwas_study||9","GCST90129648|gwas_study||6","GCST90693152|gwas_study||31"]}