| Alport Syndrome |
APRT Deficiency (APRT-D)
|
Atypical Haemolytic Uraemic Syndrome (aHUS) |
| Autosomal Dominant Polycystic Kidney Disease (ADPKD) |
Autosomal Dominant Tubulointerstitial Kidney Disease (ADTKD)
|
Autosomal Recessive Polycystic Kidney Disease (ARPKD) |
| Bartter Syndrome |
|
Calciphylaxis |
| Congenital Anomalies of the Kidneys and Urinary Tracts (CAKUT) |
|
Cystinuria |
| Dent Disease | EAST Syndrome (Epilepsy, Ataxia, Sensorineural deafness, Tubulopathy Syndrome) |
|
| Fibromuscular Dysplasia |
Gitelman and Type 3 Bartter Syndromes
|
Haemolytic Uraemic Syndrome (Shia Toxin Associated: STEC-HUS) |
| Hepatocyte Nuclear Factor 1B Mutation (HNF1b) | Hyperoxaluria (Primary Hyperoxaluria, Oxalosis) |
|
| Inherited Renal Cancer Syndromes |
|
Lowe Syndrome |
|
|
Membranous Nephropathy | Mitochondrial Disease affecting the kidney (Mitochondrial) |
| Monoclonal Gammopathy of Renal Significance (MGRS) | MPGN, DDD & C3 Glomerulopathy |
|
|
|
Pregnancy and Chronic Kidney Disease | Pure Red Cell Aplasia |
| Retroperitoneal Fibrosis | Tuberous Sclerosis |
|
