has material basis in germline mutation in UMOD familial juvenile hyperuricemic nephropathy familial juvenile hyperuricemic nephropathy type 1 https://github.com/monarch-initiative/mondo/issues/1880 https://github.com/monarch-initiative/mondo/issues/4444 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/7924 https://github.com/monarch-initiative/mondo/issues/9285 https://rarediseases.info.nih.gov/diseases/6806/familial-juvenile-hyperuricaemic-nephropathy https://www.malacards.org/card/autosomal_dominant_tubulointerstitial_kidney_disease_umod familial juvenile gouty nephropathy hyperuricemic nephropathy, familial juvenile nephropathy, familial, with gout hyperuricemic nephropathy, familial juvenile, 1 ADMCKD2 autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD SCTID:445503007 MESH:C563693 HNFJ1 MEDGEN:1645893 UMOD-related ADTKD autosomal dominant tubulointerstitial kidney disease - UMOD UMLS:C4551496 NORD:827 ADTKD-UMOD tubulointerstitial kidney disease, autosomal dominant, 1 glomerulocystic kidney disease with hyperuricemia and isosthenuria MCKD2 UMOD-associated FJHN medullary cystic kidney disease type II medullary cystic kidney disease 2 GARD:0010679 hyperuricemic nephropathy, familial juvenile, type 1 familial juvenile hyperuricemic nephropathy caused by mutation in UMOD Orphanet:209886 UMOD-related autosomal dominant tubulointerstitial kidney disease NCIT:C123172 familial nephropathy with gout UMOD familial juvenile hyperuricemic nephropathy Autosomal Dominant Tubulo-Interstitial Kidney Disease medullary cystic kidney disease 2, autosomal dominant medullary cystic kidney disease type 2 autosomal dominant medullary cystic kidney disease with hyperuricemia Orphanet:88950 gouty nephropathy, familial juvenile DOID:0061122 uromodulin storage disease autosomal dominant medullary cystic kidney disease type 2 A rare kidney disorder characterized by hyperuricemia, progressive nephropathy, and gout occurring at an early age. uromodulin-associated kidney disease OMIM:603860 UMOD-associated familial juvenile hyperuricemic nephropathy familial juvenile hyperuricaemic nephropathy OMIM:162000 UMOD-related kidney disease MONDO:0008073 OMIM:609886 FJHN type 1 autosomal dominant medullary cystic kidney disease with or without hyperuricemia inborn disorder of purine metabolism