Polycystic Kidney, Autosomal DominantTRPP Cation ChannelsPolycystic Kidney DiseasesPolycystic Kidney, Autosomal RecessiveKidneyPolycystic Ovary SyndromeKidney DiseasesGlycogen Storage Disease Type ICystsCiliaPhenotypeKidney Diseases, CysticKidney Failure, ChronicCharcot-Marie-Tooth DiseaseKidney TubulesCaroli DiseaseGlycogen Storage Disease Type IIChromosomes, Human, Pair 16Glomerular Filtration RateGlycogen Storage Disease Type IIIMutationCyst FluidDisease Models, AnimalRenal Insufficiency, ChronicDisease ProgressionLiver DiseasesRats, Mutant StrainsPedigreeGlycogen Storage Disease Type IVKidney Function TestsOrofaciodigital SyndromesKidney TransplantationProteinsKidney Tubules, CollectingNiemann-Pick DiseasesGenetic LinkageGaucher DiseaseMolecular Sequence DataNiemann-Pick Disease, Type CReceptors, VasopressinEpithelial CellsProteinuriaHypertension, RenalCreatinineGenes, DominantIothalamic AcidMembrane ProteinsHyperandrogenismHematuriaGlycogen Storage DiseaseOrgan SizeCiliary Motility DisordersMice, Mutant Strains