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)	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	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