The following table shows which cohort to enter each patient into on RaDaR.
| Diagnosis | RaDaR Cohort |
| Adenine Phosphoribosyltransferase Deficiency (APRT-D) | APRT Deficiency |
| AH amyloidosis | MGRS |
| AHL amyloidosis | MGRS |
| AL amyloidosis | MGRS |
| Alport Syndrome Carrier - Female heterozygote for X-linked Alport Syndrome (COL4A5) | Alport |
| Alport Syndrome Carrier - Heterozygote for Autosomal Alport Syndrome (COL4A3, COL4A4) | Alport |
| Alport Syndrome | Alport |
| Anti-Glomerular Basement Membrane Disease (Goodpastures) | Vasculitis |
| Atypical Haemolytic Uraemic Syndrome (aHUS) | aHUS |
| Autoimmune distal renal tubular acidosis | Tubulopathy |
| Autosomal recessive distal renal tubular acidosis | Tubulopathy |
| Autosomal recessive proximal renal tubular acidosis | Tubulopathy |
| Autosomal Dominant Polycystic Kidney Disease (ADPKD) | ADPKD |
| Autosomal Dominant Tubulointerstitial Kidney Disease (ADTKD) | ADTKD |
| Autosomal Recessive Polycystic Kidney Disease (ARPKD) | ARPKD/NPHP |
| Bartters Syndrome | Tubulopathy |
| BK Nephropathy | BK Nephropathy |
| C3 Glomerulopathy | MPGN |
| C3 glomerulonephritis with monoclonal gammopathy | MGRS |
| Calciphylaxis | Calciphylaxis |
| Crystalglobulinaemia | MGRS |
| Crystal-storing histiocytosis | MGRS |
| Cystinosis | Cystinosis |
| Cystinuria | Cystinuria |
| Dense Deposit Disease (DDD) | MPGN |
| Dent Disease | Dent & Lowe |
| Denys-Drash Syndrome | INS |
| Dominant hypophosphatemia with nephrolithiasis or osteoporosis | Tubulopathy |
| Drug induced Fanconi syndrome | Tubulopathy |
| Drug induced hypomagnesemia | Tubulopathy |
| Drug induced Nephrogenic Diabetes Insipidus | Tubulopathy |
| Epilepsy, Ataxia, Sensorineural deafness, Tubulopathy (EAST) Syndrome | Tubulopathy |
| Fabry Disease | Fabry |
| Familial Hypomagnesaemia with hypercalciuria and nephrocalcinosis | Tubulopathy |
| Familial primary hypomagnesemia with hypocalcuria | Tubulopathy |
| Familial primary hypomagnesemia with normocalcuria EGF | Tubulopathy |
| Familial renal glucosuria | Tubulopathy |
| Fanconi Renotubular syndrome 1 (FRTS1) | Tubulopathy |
| Fanconi Renotubular syndrome 2 (FRTS2) | Tubulopathy |
| Fanconi Renotubular syndrome 3 (FRTS3) | Tubulopathy |
| Fibrillary Glomerulonephritis | MGRS |
| Fibromuscular Dysplasia | Fibromuscular Dysplasia |
| Focal Segmental Glomerulosclerosis (FSGS) | INS |
| Generalized pseudohypoaldosteronism type 1 | Tubulopathy |
| Giant Vessel Arteritis | Vasculitis |
| Gitelman Syndrome | Tubulopathy |
| Glomerulocystic Disease | HNF1b |
| Heavy metal induced Fanconi syndrome | Tubulopathy |
| Hepatocyte Nuclear Factor-1 Beta Mutations (HNF1B) | HNF1b |
| Hereditary renal hypouricemia | Tubulopathy |
| Tubulopathy | |
| Hyperuricaemic Nephropathy | ADTKD |
| IgA Nephropathy | IgA Nephropathy |
| IgA Vasculitis (Henoch Schonlein) | Vasculitis |
| Inherited Renal Cancer Syndromes | Renal Cancer Inherited |
| Immunotactoid/Glomerulonephritis with Organised Microtubular Monoclonal Immunoglobulin Deposits (GOMMID) | MGRS |
| Inherited/Genetic Diabetes Mellitus Type II (MODY) | HNF1b |
| Intracapillary monoclonal IgM without cryoglobulin | MGRS |
| Intraglomerular/capillary lymphoma/leukaemia | MGRS |
| Isolated autosomal dominant hypomagnesemia, Glaudemans type | Tubulopathy |
| Large Vessel Vasculitis | Vasculitis |
| Liddle Syndromes | Tubulopathy |
| Light chain cast nephropathy | MGRS |
| Light chain proximal tubulopathy, crystalline | MGRS |
| Light chain proximal tubulopathy, non crystalline | MGRS |
| Lowe Syndrome | Dent & Lowe |
| Medium Vessel Vasculitis | Vasculitis |
| Medullary Cystic Kidney Disease | ADTKD |
| Membranous Nephropathy | Membranous Nephropathy |
| Membranoproliferative Glomerulonephritis (MPGN) | MPGN |
| Minimal Change Nephropathy | INS |
| Mitochondrial Renal Disease | Mitochondrial |
| Monoclonal Immunoglobulin Deposition Disease (MIDD; includes Light Chain Deposition Disease - LCDD; Heavy Chair Deposition Disease - HCDD; and Light and Heavy Chain Deposition Disease - LHCDD) | MGRS |
| Multicystic Dysplastic Kidneys | HNF1b |
| Nail Patella Syndrome | INS |
| Nephrogenic diabetes insipidus | Tubulopathy |
| Nephrogenic syndrome of inappropriate antidiuresis | Tubulopathy |
| Nephronophthisis (NPHP) | ARPKD/NPHP |
| Oncogenic osteomalacia | Tubulopathy |
| Osteopetrosis with renal tubular acidosis | Tubulopathy |
| Pregnancy and Chronic Kidney Disease | Pregnancy |
| Pregnancy & Lupus Nephritis | Pregnancy |
| Pregnancy in a Renal Transplant Recipient | Pregnancy |
| Primary hypomagnesemia with secondary hypocalcemia | Tubulopathy |
| Primary Hyperoxaluria | Hyperoxaluria |
| Primary Renal Fanconi Syndrome | Dent & Lowe |
| Proliferative glomerulonephritis with monoclonal immunoglobulin deposits – PGNMID | MGRS |
| Proximal tubulopathy without crystals | MGRS |
| Pseudohypoaldosteronism type 2A | Tubulopathy |
| Pseudohypoaldosteronism type 2B | Tubulopathy |
| Pseudohypoaldosteronism type 2C | Tubulopathy |
| Pseudohypoaldosteronism type 2D | Tubulopathy |
| Pseudohypoaldosteronism type 2E | Tubulopathy |
| Pure Red Cell Aplasia | PRCA |
| Renal Cysts & Diabetes Syndrome | HNF1b |
| Retroperitoneal Fibrosis | Retroperitoneal Fibrosis |
| Shiga Toxin Associated Haemolytic Uraemic Syndrome (HUS) | STEC HUS |
| Renal pseudohypoaldosteronism type 1 | Tubulopathy |
| Small Vessel Vasculitis (ANCA Associated) | Vasculitis |
| Steroid Resistant Nephrotic Syndrome (SRNS) | INS |
| Steroid Sensitive Nephrotic Syndrome (SSNS) | INS |
| Thin Basement Membrane Nephropathy | Alport |
| Thrombotic Microangiopathy with monoclonal gammopathy | MGRS |
| Tuberous Sclerosis | Tuberous Sclerosis |
| Type 1 cryoglobulinaemic Glomerulonephritis | MGRS |
| Uromodulin-Associated Nephropathy (Familial Juvenile Hyperuricaemic Nephropathy) | ADTKD |
| Unclassified Monoclonal Gammopathy of Renal Significance | MGRS |
| Variable Vessel Vasculitis | Vasculitis |
| Vasculitis | Vasculitis |
Please note
Patients who have also consented for the NephroS study should be entered under INS first and then NephroS
