Clinician Information

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
Pregnancy and Chronic Kidney Disease	Pure Red Cell Aplasia	Retroperitoneal Fibrosis
Tuberous Sclerosis	Vasculitis

Guidelines