Tubulopathies
« Back to disease groups
Primary renal tubular acidosisProximal renal tubular acidosisAutosomal dominant proximal renal tubular acidosisAutosomal recessive proximal renal tubular acidosisOsteopetrosis with renal tubular acidosisDistal renal tubular acidosisAutosomal dominant distal renal tubular acidosis (dRTA)Autosomal recessive distal renal tubular acidosis (dRTA)Distal renal tubular acidosis with hemolytic anemiaAuto-immune distal renal tubular acidosisSjogren SyndromePrimary biliary cholangitisAutoimmune hepatitisOther autoimmune dRTACystinuriaHypotonia-cystinuria syndromeBartter syndromeHypokalemic alkalosis, CLDN10 associated Gitelman syndromeGitelman-like syndromeGenetic primary hypomagnesemiaFamilial primary hypomagnesemia with hypercalciuria and nephrocalcinosisFamilial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvementFamilial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvementGenetic primary hypomagnesemia with normocalcuriaFamilial primary hypomagnesemia with normocalciuria and normocalcemiaIsolated autosomal dominant hypomagnesemia, Glaudemans typePrimary hypomagnesemia with secondary hypocalcemiaFamilial primary hypomagnesemia with hypocalcuriaAutosomal dominant primary hypomagnesemia with hypocalciuriaPrimary hypomagnesemia with refractory seizures and intellectual disabilityHypomagnesaemia, drug-inducedFanconi syndrome, primaryFanconi syndrome, drug inducedFanconi syndrome, Cisplatin inducedFanconi syndrome, induced by other drugFanconi syndrome, heavy metal inducedFanconi syndrome, lead inducedFanconi syndrome, mercury inducedFaconi syndrome, induced by other heavy metalFanconi syndrome, monoclonal Ig light chain-associatedHypophosphatemic ricketsX-linked hypophosphatemic rickets (XLHR)Autosomal recessive hypophosphatemic ricketsAutosomal dominant hypophosphatemic ricketsHereditary hypophosphatemic rickets with hypercalciuriaHypophosphatemia, dominant, with nephrolithiasis or osteoporosisHypercalciuria, idiopathicOncogenic osteomalaciaNephrogenic diabetes insipidusNephrogenic syndrome of inappropriate antidiuresisTubulointerstitial nephritis and uveitis syndromeFamilial renal glucosuriaPseudohypoaldosteronism type 1Generalized pseudohypoaldosteronism type 1Renal pseudohypoaldosteronism type 1EAST syndromeArthrogryposis-renal dysfunction-cholestasis (ARC) syndromeAutosomal dominant hypocalcemiaHereditary renal hypouricemia
No matches
« Back to disease groups
Glomerulopathies
Tubulopathies
Thrombotic microangiopathies
Metabolic nephropathies
Renal or urinary tract malformations
Familial cystic renal diseases
Any rare kidney disease (A-Z)
Patient Information Materials