Clinician Information | UK Kidney Association

Information for clinicians is available, for the conditions currently recruiting for the RaDaR rare disease registry.

Alport Syndrome

APRT Deficiency

APRT-D

Atypical Haemolytic Uraemic Syndrome

Autosomal Dominant Polycystic Kidney Disease

ADPKD

Autosomal Dominant Tubulointerstitial Kidney Disease

Autosomal Recessive Polycystic Kidney disease

Bartter Syndrome Type 3

Bartter Syndromes Types 1, 2 & 4

BK Nephropathy

Calciphylaxis

CKD due to Genetic Factors in people of African ancestry

CKD-Africa

Congenital Anomalies of the Kidneys and Urinary Tracts

CAKUT

Cystinosis

Cystinuria

Dent Disease

EAST Syndrome

Epilepsy, Ataxia, Sensorineural deafness, Tubulopathy Syndrome

Fabry Disease

Fibromuscular Dysplasia

Gitelman Syndrome

Haemolytic Uraemic Syndrome

Shia Toxin Associated: STEC-HUS

Hepatic Nuclear Factor 1B mutation

HNF1b

Hyperoxaluria

Primary Hyperoxaluria, Oxalosis

IgA Nephropathy

Inherited Renal Cancer Syndromes

Liddle Syndrome

Lowe Syndrome

Lupus Nephritis

Membranous Nephropathy

Mitochondrial disease affecting the kidney

Mitochondrial

Monoclonal Gammopathy of Renal Significance

MGRS

MPGN, DDD & C3 Glomerulopathy

Nephronophthisis

Nephrotic Syndrome

Post-transplant Cytomegalovirus

CMV

Pregnancy and Chronic Kidney Disease

Pure Red Cell Aplasia

Retroperitoneal Fibrosis

Tuberous Sclerosis

Vasculitis