| Disease Aliases (26) | Adtkd-umod Adtkd1 Autosomal dominant medullary cystic kidney disease type 2 Autosomal dominant medullary cystic kidney disease with hyperuricemia Autosomal dominant tubulo-interstitial kidney disease Autosomal dominant tubulointerstitial kidney disease - umod Autosomal dominant tubulointerstitial kidney disease due to mutations in umod Familial juvenile hyperuricemic nephropathy caused by mutation in umod Fjhn type 1 Glomerulocystic kidney disease with hyperuricemia and isosthenuria Hnfj1 Hyperuricemic nephropathy, familial juvenile, 1 Hyperuricemic nephropathy, familial juvenile, type 1 Mckd2 Medullary cystic kidney disease 2 Medullary cystic kidney disease type 2 Medullary cystic kidney disease type ii Tubulointerstitial kidney disease, autosomal dominant, 1 Umod familial juvenile hyperuricemic nephropathy Umod-associated familial juvenile hyperuricemic nephropathy Umod-associated fjhn Umod-associated kidney disease Umod-related adtkd Umod-related autosomal dominant tubulointerstitial kidney disease Umod-related kidney disease Uromodulin storage disease |
Associated Genes (0) | |||||||
| Cross-references of Familial juvenile hyperuricemic nephropathy type 1 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |