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 |