RaDaR is open for recruitment for children and adults with the following conditions.
Please use this list in conjunction with the Inclusion / Exclusion criteria - not every patient with one or more of these diagnoses will be eligible for RaDaR.
| Condition / Diagnosis | Rare Disease Group / Cohort |
| Aarskog-Scott Syndrome | Calciphylaxis |
| Adult nephrotic syndrome - no histology | CKD due to Genetic Factors in people of African ancestry |
| Adult nephrotic syndrome - no histology | Idiopathic Nephrotic Syndrome |
| AH amyloidosis | Monoclonal Gammopathy of Renal Significance |
| AHL amyloidosis | Monoclonal Gammopathy of Renal Significance |
| AL amyloidosis | Monoclonal Gammopathy of Renal Significance |
| Alport Syndrome | Alport Syndrome |
| Alport Syndrome - Histologically Proven | Alport Syndrome |
| Alport Syndrome - No Histology | Alport Syndrome |
| Anti-Glomerular Basement Membrane (GBM) Disease (Goodpastures) | Vasculitis |
| APRT Deficiency | APRT Deficiency |
| Atypical Haemolytic Uraemic Syndrome (AHUS) | Atypical Haemolytic Uraemic Syndrome |
| Autoimmune distal renal tubular acidosis | Tubulopathy |
| Autosomal dominant distal renal tubular acidosis | Tubulopathy |
| Autosomal Dominant Polycystic Kidney Disease | Autosomal Dominant Polycystic Kidney Disease |
| Autosomal Dominant Tubulointerstitial Kidney Disease (FUANS) | Autosomal Dominant Tubulointerstitial Kidney Disease (FUAN) |
| Autosomal recessive distal renal tubular acidosis | Tubulopathy |
| Autosomal Recessive Polycystic Kidney Disease | Autosomal Recessive Polycystic Kidney Disease/Nephronophthisis |
| Autosomal recessive proximal renal tubular acidosis | Tubulopathy |
| BAP1-related tumour predisposition syndrome | Inherited Renal Cancer Syndromes |
| Bartter syndrome | Tubulopathy |
| Bartter Syndrome - Type 2 | Tubulopathy |
| Bartter Syndrome - Type 3 | Tubulopathy |
| Bartter Syndrome - Type 4a | Tubulopathy |
| Bartter Syndrome - Type 4b | Tubulopathy |
| Birt Hogg Dube syndrome | Inherited Renal Cancer Syndromes |
| BK Virus in Transplant Patient | BK Nephropathy |
| Bladder exstrophy | Congenital Anomalies of the Kidneys and Urinary Tracts |
| C3 Glomerulonephritis | Membranoproliferative Glomerulonephritis |
| C3 glomerulonephritis with monoclonal gammopathy | Monoclonal Gammopathy of Renal Significance |
| Calciphylaxis | Calciphylaxis |
| Chronic hypertensive nephropathy - histologically proven | CKD due to Genetic Factors in people of African ancestry |
| Chronic hypertensive nephropathy - no histology | CKD due to Genetic Factors in people of African ancestry |
| Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - histologically proven | CKD due to Genetic Factors in people of African ancestry |
| Chronic kidney disease (CKD) / chronic renal failure (CRF) - aetiology uncertain / unknown - no histology | CKD due to Genetic Factors in people of African ancestry |
| CKD1 | Pregnancy |
| CKD2 | Pregnancy |
| CKD3 | Pregnancy |
| CKD4 | Pregnancy |
| CKD5 | Pregnancy |
| Cloacal Exstrophy | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Congenital Anomaly Of The Kidney | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Congenital Anomaly Of The Urinary Tract Proper | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Congenital Hydronephrosis | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Congenital Megaureter | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Congenital nephrotic syndrome (CNS) - no histology | Idiopathic Nephrotic Syndrome |
| Congenital Posterior Urethral Valves | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Congenital vesico-ureteric junction obstruction | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Cryoglobulinaemic vasculitis | Vasculitis |
| Crystalglobulinaemia | Monoclonal Gammopathy of Renal Significance |
| Crystal-storing histiocytosis | Monoclonal Gammopathy of Renal Significance |
| Cutaneous Vasculitis | Vasculitis |
| Cystic Renal Dysplasia | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Cystinosis | Cystinosis |
| Cystinuria | Cystinuria |
| Cytomegalovirus (CMV) infection post transplant | CMV Post Transplant |
| Dense Deposit Disease (DDD) | Membranoproliferative Glomerulonephritis |
| Dent Disease | Dent Disease and Lowe Syndrome |
| Dent Disease and Lowe Syndrome | Dent Disease and Lowe Syndrome |
| Denys-Drash syndrome | Idiopathic Nephrotic Syndrome |
| Diabetes - Type II MODY - Inherited/Genetic | HNF1b Mutations |
| Dominant hypophosphatemia with nephrolithiasis or osteoporosis | Tubulopathy |
| Drug induced Fanconi syndrome | Tubulopathy |
| Drug induced hypomagnesemia | Tubulopathy |
| Drug induced Nephrogenic Diabetes Insipidus | Tubulopathy |
| Duplex Kidney | Congenital Anomalies of the Kidneys and Urinary Tracts |
| EAST Syndrome | Tubulopathy |
| Ectopic Kidney | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Ectopic Ureter | Congenital Anomalies of the Kidneys and Urinary Tracts |
| End Stage Renal Failure (ESRF) - Unknown cause | CKD due to Genetic Factors in people of African ancestry |
| Eosinophilic granulomatosis with polyangiitis (Chrug-Strauss syndrome) | Vasculitis |
| Exstrophy Epispadias Complex | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Fabry disease - histologically proven | Fabry Disease |
| Fabry disease - no histology | Fabry Disease |
| Familial hypomagnesaemia | Tubulopathy |
| Familial Hypomagnesaemia with hypercalciuria and nephrocalcinosis CLDN16/19 | Tubulopathy |
| Fanconi Renotubular syndrome 1 (FRTS1) | Tubulopathy |
| Fanconi Renotubular syndrome 2 (FRTS2) | Tubulopathy |
| Fanconi Renotubular syndrome 3 (FRTS3) | Tubulopathy |
| Fibrillary Glomerulonephritis | Monoclonal Gammopathy of Renal Significance |
| Fibromuscular Dysplasia | Fibromuscular Dysplasia |
| GCA Giant Cell Arteritis | Vasculitis |
| Generalized pseudohypoaldosteronism type 1 | Tubulopathy |
| Gitelman Syndrome | Tubulopathy |
| Glomerulocystic Disease | HNF1b Mutations |
| GPA Granulomatosis with Polyangiitis (formerly known as Wegner's Granulomatosis) | Vasculitis |
| Haematuria and proteinuria - no histology | CKD due to Genetic Factors in people of African ancestry |
| Heavy metal induced Fanconi syndrome | Tubulopathy |
| Hereditary hypophosphatemic rickets with hypercalciuria | Tubulopathy |
| Hereditary leiomyomatosis and renal cell cancer syndrome(HLRCC) | Inherited Renal Cancer Syndromes |
| Hereditary Type 1 papillary renal cell carcinoma syndrome (MET oncogene) | Inherited Renal Cancer Syndromes |
| HNF1b Mutations | HNF1b Mutations |
| Hyperoxaluria | Hyperoxaluria |
| Hyperuricaemic Nephropathy | Autosomal Dominant Tubulointerstitial Kidney Disease (FUAN) |
| Hypocomplementemic urticarial vasculitis | Vasculitis |
| Hypophosphataemic rickets autosomal recessive (AR) | Tubulopathy |
| Hypophosphataemic rickets X-linked (XL) | Tubulopathy |
| Idiopathic inherited Renal Cell Carcinoma syndrome | Inherited Renal Cancer Syndromes |
| Idiopathic Nephrotic Syndrome | Idiopathic Nephrotic Syndrome |
| IgA Nephropathy | IgA Nephropathy |
| IgA Vasculitis (Henoch Schonlein) | Vasculitis |
| Immune-Complex MPGN | Membranoproliferative Glomerulonephritis |
| Immunotactoid/Glomerulonephritis with Organised Microtubular Monoclonal Immunoglobulin Deposits (GOMMID) | Monoclonal Gammopathy of Renal Significance |
| INS - Steroids NOT Tried | Idiopathic Nephrotic Syndrome |
| Intracapillary monoclonal IgM without cryoglobulin | Monoclonal Gammopathy of Renal Significance |
| Intraglomerular/capillary lymphoma/leukaemia | Monoclonal Gammopathy of Renal Significance |
| Isolated autosomal dominant hypomagnesemia, Glaudemans type | Tubulopathy |
| Large Vessel Vasculitis | Vasculitis |
| Liddle Syndrome | Tubulopathy |
| Light chain cast nephropathy | Monoclonal Gammopathy of Renal Significance |
| Light chain proximal tubulopathy, crystalline | Monoclonal Gammopathy of Renal Significance |
| Light chain proximal tubulopathy, non crystalline | Monoclonal Gammopathy of Renal Significance |
| Lowe Syndrome (Oculocerebrorenal Syndrome) | Dent Disease and Lowe Syndrome |
| Lupus Nephritis | Lupus Nephritis |
| Lupus Nephritis | Pregnancy |
| Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - histologically proven | CKD due to Genetic Factors in people of African ancestry |
| Malignant hypertensive nephropathy / accelerated hypertensive nephropathy - no histology | CKD due to Genetic Factors in people of African ancestry |
| Medium Vessel Vasculitis | Vasculitis |
| Medullary Cystic Kidney Disease | Autosomal Dominant Tubulointerstitial Kidney Disease (FUAN) |
| Membranous Nephropathy | Membranous Nephropathy |
| Mesangial proliferative glomerulonephritis | Idiopathic Nephrotic Syndrome |
| Mitochondrial Disease | Mitochondrial Renal Disease |
| Monoclonal Immunoglobulin Deposition Disease (MIDD, includes LCDD, HCDD and LHCDD) | Monoclonal Gammopathy of Renal Significance |
| MPA Microscopic Polyangiitis | Vasculitis |
| MPGN/C3G-NOS | Membranoproliferative Glomerulonephritis |
| Multicystic Dysplastic Kidneys | HNF1b Mutations |
| Nephrogenic diabetes insipidus | Tubulopathy |
| Nephrogenic syndrome of inappropriate antidiuresis | Tubulopathy |
| Nephronophthisis | Autosomal Recessive Polycystic Kidney Disease/Nephronophthisis |
| Nephropathy related to HIV - histologically proven | CKD due to Genetic Factors in people of African ancestry |
| Nephropathy related to HIV - no histology | CKD due to Genetic Factors in people of African ancestry |
| Other forms of primary systemic vasculitis including single organ vasculitis | Vasculitis |
| Other Primary Renal Fanconi Syndrome | Dent Disease and Lowe Syndrome |
| Pelviureteric Junction Obstruction | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Pregnancy | Pregnancy |
| Primary CNS vasculitis | Vasculitis |
| Primary focal segmental glomerulosclerosis (FSGS) | CKD due to Genetic Factors in people of African ancestry |
| Primary Hyperoxaluria | Hyperoxaluria |
| Primary Hyperoxaluria Type I | Hyperoxaluria |
| Primary Hyperoxaluria Type II | Hyperoxaluria |
| Primary hyperoxaluria type III | Hyperoxaluria |
| Primary hypomagnesemia with secondary hypocalcemia | Tubulopathy |
| Proliferative glomerulonephritis with monoclonal immunoglobulin deposits (PGNMID) | Monoclonal Gammopathy of Renal Significance |
| Prune Belly Syndrome | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Pseudohypoaldosteronism type 2A | Tubulopathy |
| Pseudohypoaldosteronism type 2B | Tubulopathy |
| Pseudohypoaldosteronism type 2C | Tubulopathy |
| Pseudohypoaldosteronism type 2D | Tubulopathy |
| Pseudohypoaldosteronism type 2E | Tubulopathy |
| PTEN hamartoma tumour syndrome (PHTS) | Inherited Renal Cancer Syndromes |
| Pure Red Cell Aplasia | Pure Red Cell Aplasia |
| Renal Agenesis | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Renal Cysts & Diabetes Syndrome | HNF1b Mutations |
| Renal Dysplasia | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Renal Hypoplasia | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Renal pseudohypoaldosteronism type 1 | Tubulopathy |
| Renal Transplant Recipient | Pregnancy |
| Retroperitoneal Fibrosis | Retroperitoneal Fibrosis |
| Sickle cell nephropathy - histologically proven | CKD due to Genetic Factors in people of African ancestry |
| Sickle cell nephropathy - no histology | CKD due to Genetic Factors in people of African ancestry |
| SRNS - Presumed Steroid Resistance | Idiopathic Nephrotic Syndrome |
| SRNS - Primary Steroid Resistance | Idiopathic Nephrotic Syndrome |
| SRNS - Secondary Steroid Resistance | Idiopathic Nephrotic Syndrome |
| SSNS - Frequently Relapsing | Idiopathic Nephrotic Syndrome |
| SSNS - Partial Steroid Resistance | Idiopathic Nephrotic Syndrome |
| SSNS - Steroid Dependant | Idiopathic Nephrotic Syndrome |
| SSNS - Steroid Sensitive | Idiopathic Nephrotic Syndrome |
| STEC-associated HUS | STEC-associated HUS |
| Succinate dehydrogenase(SDH)-related tumour predisposition syndrome | Inherited Renal Cancer Syndromes |
| Thin Basement Membrane Disease | Alport Syndrome |
| Thrombotic Microangiopathy with monoclonal gammopathy | Monoclonal Gammopathy of Renal Significance |
| Tuberous sclerosis | Tuberous Sclerosis |
| Type 1 cryoglobulinaemic Glomerulonephritis | Monoclonal Gammopathy of Renal Significance |
| Unclassified MGRS | Monoclonal Gammopathy of Renal Significance |
| Ureterocele | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Variable Vessel Vasculitis | Vasculitis |
| Vasculitis NOS | Vasculitis |
| Vesicoureteric Reflux | Congenital Anomalies of the Kidneys and Urinary Tracts |
| Von Hippel-Lindau disease | Inherited Renal Cancer Syndromes |