Rare disease groups.
| Alport syndrome |
| Autosomal recessive polcystic kidney disease |
| Adenine phosphoribosyltransferase deficiency |
| Atypical haemolytic uraemic syndrome |
| Cystinosis |
| Cystinuria |
| Dent disease and Lowe syndrome |
| Familial urate associated nephropathy (uromudulin associated nephropathy, hyperuricaemic nephropathy and medullary cystic kidney disease) |
| Hepatocyte nuclear factor-1 beta |
| Shiga toxin-associated hemolytic-uremic syndrome |
| Hyperoxaluria (primary hyperoxaluria, oxalosis) |
| Hypokalaemic alkaloses (Bartter, EAST, Gitelman and Liddle syndromes) |
| Membranous nephropathy |
| Membranoproliferative glomerulonephritis, dense deposit disease |
| Nephrotic syndrome (steroid resistant, congenital, associated with primary focal segmental glomerulosclerosis) |
| Pregnancy in chronic kidney disease |
| Pure red cell aplasia |
| Vasculitis |