| Disease Aliases (41) | Admckd2 Adtkd due to umod mutations Adtkd-umod Adtkd1 Autosomal dominant tubulointerstitial kidney disease, umod-related Autosomal dominant medullary cystic kidney disease type 2 Autosomal dominant medullary cystic kidney disease type 2 (former) Autosomal dominant tubulointerstitial kidney disease due to umod mutations Fjhn Fjhn type 1 Familial juvenile hyperuricemic nephropathy 1 Familial juvenile gouty nephropathy Familial juvenile hyperuricemic nephropathy type 1 Familial nephropathy with gout Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gouty nephropathy, familial juvenile Hnfj1 Hyperuricemic nephropathy, familial juvenile, 1 Mckd2 Medullary cystic kidney disease 2 Medullary cystic kidney disease 2, autosomal dominant Medullary cystic kidney disease 2 (former) Medullary cystic kidney disease type 2 Umod familial juvenile hyperuricemic nephropathy Umod-associated kidney disease Umod-associated fjhn Umod-associated familial juvenile hyperuricemic nephropathy Umod-related adtkd Umod-related autosomal dominant tubulointerstitial kidney disease Umod-related kidney disease Uromodulin kidney disease Uromodulin-associated kidney disease Autosomal dominant medullary cystic kidney disease with hyperuricemia Autosomal dominant tubulointerstitial kidney disease due to mutations in umod Familial juvenile hyperuricaemic nephropathy Familial juvenile hyperuricemic nephropathy caused by mutation in umod Hyperuricemic nephropathy, familial juvenile 1 Hyperuricemic nephropathy, familial juvenile, 1; hnfj1 Hyperuricemic nephropathy, familial juvenile, type 1 Uromodulin storage disease |
Associated Genes (1) NCBI-RefSeq: UMOD (Uromodulin) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Familial juvenile hyperuricemic nephropathy type 1 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |