has material basis in germline mutation in REN familial juvenile hyperuricemic nephropathy familial juvenile hyperuricemic nephropathy type 2 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/tubulointerstitial_kidney_disease_autosomal_dominant_4 HNFJ2 OMIM:613092 autosomal dominant tubulointerstitial kidney disease due to mutations in REN REN-associated FJHN MESH:C567760 early-onset hyperuricemia, Anemia, and progressive kidney failure REN-associated kidney disease DOID:0061119 SCTID:721840000 MONDO:0013128 familial juvenile hyperuricemic nephropathy type 2 MEDGEN:414347 FJHN type 2 REN-related autosomal dominant tubulointerstitial kidney disease Familial juvenile hyperuricemic nephropathy type 2 is a rare autosomal dominantly inherited disease of childhood characterized by hypoproliferative anemia, hyperuricemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system (RAS). REN familial juvenile hyperuricemic nephropathy hyperuricemic nephropathy, familial juvenile, 2 tubulointerstitial kidney disease, autosomal dominant, 4 familial juvenile hyperuricemic nephropathy caused by mutation in REN Orphanet:217330 UMLS:C2751310 REN-associated familial juvenile hyperuricemic nephropathy ADTKD-REN GARD:0013461 hyperuricemic nephropathy, familial juvenile, type 2 inherited renal tubular disease