11 beta HSD (BASKET)17 alpha HydroxylaseAcidosis (RTA1 distal)Acidosis (RTA2 proximal)AE1AlkaptonuriaAminoaciduriasAniridia Wilms syndromeAutosomal recessive rickets with craniostenosis and deafnessAVPR2Blue diaper syndromeCalcitriol resistanceCarboanhydrase IICOL4A3COL4A4COL4A5COL4A6
CYP11B2 aldosterone synthaseCystathioninuriaCytochrome 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 syndromeHypercystinuria isolatedHyperdibasic aminoaciduria IHyperhistidinuria
Hypomagnesiemia congenital primaryHypophosphatemic 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 syndromeNBC1NCCT
Nipples supernumeraryPAT1Perlman syndromePhosphatidylinositol bisphosphate phosphatasePierson Zenker syndromeProline (Hyperprolinemia)Pseudotumoral calcinosisReceptor (PTH)ROMKSchwachmann Bodian syndromeSclerema neonatorumSLC3A1SLC6A19SLC7A9Xanthinuria
Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth
All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.