RaDaR Diagnoses and Cohorts

Diagnosis (currently being updated 08/01/2024)

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
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


NICE accredited clinical practice guidelines 

Available here

25th Annual Report

Analyses about the care provided to patients at UK renal centres.

Read the report

2022 UKRR AKI Report

A report on the nationwide collection of AKI warning test scores. 

Read the report