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
- Inherited Renal Cancer Syndromes
- 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
- Mitochondrial Renal Disease
- 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
