GenTIGSA Gene Database on Rare Genetic Disorders
Familial Juvenile Hyperuricemic Nephropathy Type 1  
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