| 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 | 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 |