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.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version March 2024
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Autosomal dominant tubulointerstitial kidney disease?
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