11 beta HSD (BASKET)17 alpha HydroxylaseAcidosis (RTA1 distal)Acidosis (RTA2 proximal)AE1AlkaptonuriaAminoaciduriasAniridia Wilms syndromeAutosomal recessive rickets with craniostenosis and deafnessAVPR2Blue diaper syndromeCalcitriol resistanceCarboanhydrase IICOL4A3COL4A4COL4A5COL4A6CYP11B2 aldosterone synthase
CystathioninuriaCytochrome c oxidase deficiencyDicarboxylic aminoaciduriaEpstein s syndromefamilial hypophosphatemic osteomalaciaFructose 1 phosphate aldolaseGalactose 1 phosphate uridyl transferaseGALNT3Gluco GlycinuriaGlucosuria with renal phosphate diabetesH ATPase A4 subunitH ATPase B1 subunitHartnup s syndromeHomogentisic acid oxidaseHypercystinuria isolatedHyperdibasic aminoaciduria IHyperhistidinuriaHypomagnesiemia congenital primary
Hypophosphatemic nonrachitic bone diseaseIminoglycinuriaJadassohn s linear sebaceous nevusJansen s diseaseKidney (CNS Finnish type)Kidney (Collagenofibrotic nephropathy)Kidney (Diffuse mesangial sclerosis)Kidney (Fibronectin Glomerulopathy)Kidney (Hematuria benign)LAMB2 Laminin beta2LMX1BMERRFMULIBREY dysplasiaNARP syndromeNBC1NCCTNipples supernumeraryOchronosis
PAT1Perlman syndromePhosphatidylinositol bisphosphate phosphatasePierson Zenker syndromeProline (Hyperprolinemia)Pseudotumoral calcinosisReceptor (PTH)ROMKSchwachmann Bodian syndromeSclerema neonatorumSLC3A1SLC6A19SLC7A9Xanthinuria
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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.