Rare Disease Groups | UK Kidney Association

Some rare disease groups cover several similarly classed conditions together.

Alport Syndrome

APRT Deficiency

APRT-D

ARPKD & NPHP

Autosomal Recessive Polycystic Kidney Disease & Nephronophthisis

Atypical Haemolytic Uraemic Syndrome

aHUS

Autosomal Dominant Polycystic Kidney Disease

ADPKD

Autosomal Dominant Tubulointerstitial Kidney Disease

ADTKD

BK Nephropathy

Calciphylaxis

CKD due to Genetic Factors in people of African ancestry

CKD-Africa Genes

Congenital Anomalies of the Kidneys and Urinary Tracts

CAKUT

Cystinosis

Cystinuria

Dent Disease & Lowe Syndrome

Fabry Disease

Fibromuscular Dysplasia

Haemolytic Uraemic Syndrome

Shiga Toxin Associated; STEC-HUS

Hepatic Nuclear Factor 1B Mutation

HNF1b

Hyperoxaluria

Primary Hyperoxaluria, Oxalosis

IgA Nephropathy

Inherited Renal Cancer Syndromes

Lupus Nephritis

Membranous Nephropathy

Mitochondrial disease affecting the kidney

Monoclonal Gammopathy of Renal Significance

MGRS

MPGN, DDD & C3 Glomerulopathy

Membranoproliferative Glomerulonephritis, Dense Deposit Disease & C3 Glomerulopathy

Nephrotic Syndrome

Steroid Sensitive & Steroid Resistant; SSNS & SRNS

Post-transplant Cytomegalovirus

CMV

Pregnancy and Chronic Kidney Disease

Pure Red Cell Aplasia

PRCA

Retroperitoneal Fibrosis

Tuberous Sclerosis

Tubulopathy

Vasculitis