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Hyperuricemic nephropathy, familial juvenile type 3

Summary

Familial juvenile hyperuricemia nephropathy-3 may be a distinct form of autosomal dominant tubulointerstitial kidney disease (ADTKD); however, because the mapping of the disorder in the families described by Piret et al. (2011) is tentative, it is possible that the families have a form of the disorder described in the ADTKD series (see ADTKD1, 162000). [from OMIM]

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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