11 beta HSD (BASKET)17 alpha HydroxylaseAcidosis (RTA1 distal)Acidosis (RTA2 proximal)Action Myoclonus Renal Failure SyndromeACTN4 Alpha actinin4AE1AlkaptonuriaAminoaciduriasAniridia Wilms syndromeAutosomal recessive rickets with craniostenosis and deafnessAVPR2Blue diaper syndromeCalcitriol resistanceCarboanhydrase IICD151 TetraspaninCD2APCoenzyme Q10COL4A3COL4A4COL4A5COL4A6Congenital nephrotic syndrome finnish typeCOQ2CYP11B2 aldosterone synthaseCystathioninuria
Cytochrome c oxidase deficiencyDenys Drash syndromeDicarboxylic aminoaciduriaEarly onset familial nephrotic syndromeEpstein s syndromefamilial hypophosphatemic osteomalaciaFechtner s syndromeFrasier s syndromeFructose 1 phosphate aldolaseGalactose 1 phosphate uridyl transferaseGalloway Mowat s syndromeGALNT3Gluco GlycinuriaGlucosuria with renal phosphate diabetesGMS1H ATPase A4 subunitH ATPase B1 subunitHartnup s syndromeHypercystinuria isolatedHyperdibasic aminoaciduria IHyperhistidinuriaHypomagnesiemia congenital primaryHypophosphatemic nonrachitic bone diseaseIminoglycinuriaJadassohn s linear sebaceous nevusJansen s disease
Kidney (CNS Finnish type)Kidney (Collagenofibrotic nephropathy)Kidney (Diffuse mesangial sclerosis)Kidney (Fibronectin Glomerulopathy)Kidney (FSGS)Kidney (Hematuria benign)LAMB2 Laminin beta2LamininLMNA Lamin C Prelamin ALMX1BMandibuloacral dysplasiaMay Hegglin anomalyMERRFMULIBREY dysplasiaMYH9Nail patella syndromeNARP syndromeNBC1NCCTNipples supernumeraryNPHS1 NephrinNPHS2PAT1Perlman syndromePhosphatidylinositol bisphosphate phosphatasePhospholipase C epsilon
Pierson s syndromePierson Zenker syndromePLCE1PodocinProline (Hyperprolinemia)Pseudotumoral calcinosisReceptor (PTH)ROMKSCARB2Schimke immunoosseous dysplasiaSchwachmann Bodian syndromeSclerema neonatorumSebastian s syndromeSLC3A1SLC6A19SLC7A9SMARCALISteroid resistant nephrotic syndrome SRN1TRPC6WT1XanthinuriaZMPSTE24
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