Autosomal dominant tubulointerstitial kidney disease

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Autosomal dominant tubulointerstitial kidney disease

Synonyms: ADTKD | Familial juvenile hyperuricemic nephropathy | MCKD | Medullary cystic kidney disease

A rare genetic renal tubular disease characterized by tubular damage and interstitial fibrosis in absence of glomerular lesions and clinically manifesting with chronic kidney disease (CKD) and slow progression to end-stage kidney disease (ESKD).

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 Data version March 2024

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Autosomal dominant tubulointerstitial kidney disease?

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Clinical Trials

For a list of clinical trials in this disease area, please click here.