REN-related autosomal dominant tubulointerstitial kidney disease
Synonyms: ADTKD-REN | FJHN type 2 | Familial juvenile hyperuricemic nephropathy type 2 | REN-associated FJHN | REN-associated familial juvenile hyperuricemic nephropathy | REN-associated kidney disease
A rare autosomal dominant tubulointerstitial kidney disease (ADTKD) of childhood due to REN mutations and characterized by early onset hypoproliferative anemia hyperuricemia gout and slowly progressive tubulointerstitial kidney disease.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
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REN-related autosomal dominant tubulointerstitial kidney disease?
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Advocacy Organizations
Help Hope Live
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Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
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