Current Recruitment

RaDaR is open for recruitment for children and adults with the following conditions:

  • Adenine Phosphoribosyltransferase Deficiency (APRT-D)
  • AH amyloidosis
  • AHL amyloidosis
  • AL amyloidosis
  • Alport Syndrome
  • Atypical Haemolytic Uraemic Syndrome (aHUS)
  • Autoimmune distal renal tubular acidosis
  • Autosomal recessive distal renal tubular acidosis
  • Autosomal recessive proximal renal tubular acidosis
  • Autosomal Dominant Polycystic Kidney Disease (ADPKD)
  • Autosomal Recessive Polycystic Kidney Disease (ARPKD)
  • Bartters Syndrome
  • BK Nephropathy
  • C3 glomerulonephritis with monoclonal gammopathy
  • C3 Glomerulopathy
  • Calciphylaxis
  • Crystalglobulinaemia
  • Crystal-storing histiocytosis
  • Cystinosis
  • Cystinuria
  • Dense Deposit Disease (DDD)
  • Dent Disease
  • Denys-Drash Syndrome
  • Dominant hypophosphatemia with nephrolithiasis or osteoporosis
  • Drug induced Fanconi syndrome
  • Drug induced hypomagnesemia
  • Drug induced Nephrogenic Diabetes Insipidus
  • Epilepsy, Ataxia, Sensorineural deafness, Tubulopathy Syndrome (EAST)
  • Fabry Disease
  • Familial Hypomagnesaemia with hypercalciuria and nephrocalcinosis
  • Familial primary hypomagnesemia with hypocalcuria
  • Familial primary hypomagnesemia with normocalcuria EGF
  • Familial renal glucosuria
  • Fanconi Renotubular syndrome 1 (FRTS1)
  • Fanconi Renotubular syndrome 2 (FRTS2)
  • Fanconi Renotubular syndrome 3 (FRTS3)
  • Fibrillary Glomerulonephritis
  • Fibromuscular Dysplasia
  • Focal Segmental Glomerulosclerosis (FSGS)
  • Generalized pseudohypoaldosteronism type 1
  • Gitelman Syndrome
  • Heavy metal induced Fanconi syndrome
  • Hepatocyte Nuclear Factor-1 Beta Mutations (HNF1B)
  • Hereditary renal hypouricemia
  • Hereditary hypophosphatemic rickets with hypercalciuria
  • Hyperuricaemic Nephropathy
  • IgA Nephropathy
  • Immunotactoid/Glomerulonephritis with Organised Microtubular Monoclonal Immunoglobulin Deposits (GOMMID)
  • Intracapillary monoclonal IgM without cryoglobulin
  • Intraglomerular/capillary lymphoma/leukaemia
  • Isolated autosomal dominant hypomagnesemia, Glaudemans type
  • Liddle Syndromes
  • Light chain cast nephropathy
  • Light chain proximal tubulopathy, crystalline
  • Light chain proximal tubulopathy, non crystalline
  • Lowe Syndrome
  • Membranous Nephropathy
  • Membranoproliferative Glomerulonephritis (MPGN)
  • Medullary Cystic Kidney Disease
  • Minimal Change Nephropathy
  • Monoclonal Immunoglobulin Deposition Disease (MIDD; includes Light Chain Deposition Disease – LCDD; Heavy Chair Deposition Disease – HCDD; and Light and Heavy Chain Deposition Disease – LHCDD)
  • Nail Patella Syndrome
  • Nephrogenic diabetes insipidus
  • Nephrogenic syndrome of inappropriate antidiuresis
  • Nephronophthisis (NPHP)
  • Oncogenic osteomalacia
  • Osteopetrosis with renal tubular acidosis
  • Pregnancy and Chronic Kidney Disease
  • Primary hypomagnesemia with secondary hypocalcemia
  • Primary Hyperoxaluria
  • Proliferative glomerulonephritis with monoclonal immunoglobulin deposits – PGNMID
  • Proximal tubulopathy without crystals
  • Pseudohypoaldosteronism type 2A
  • Pseudohypoaldosteronism type 2B
  • Pseudohypoaldosteronism type 2C
  • Pseudohypoaldosteronism type 2D
  • Pseudohypoaldosteronism type 2E
  • Pure Red Cell Aplasia
  • Renal pseudohypoaldosteronism type 1
  • Retroperitoneal Fibrosis
  • Shiga Toxin Associated Haemolytic Uraemic Syndrome (HUS)
  • Steroid Resistant Nephrotic Syndrome (SRNS)
  • Steroid Sensitive Nephrotic Syndrome (SSNS)
  • Thin Basement Membrane Nephropathy
  • Thrombotic Microangiopathy with monoclonal gammopathy
  • Type 1 cryoglobulinaemic Glomerulonephritis
  • Tuberous Sclerosis
  • Unclassified Monoclonal Gammopathy of Renal Significance (MGRS)
  • Vasculitis
RaDaR Current Conditions Version 5 Updated October 2019
Written by the Rarerenal.org Operational Management Board