Nephrolithiasis / nephrocalcinosis / medullary sponge kidney | 815 | Familial focal segmental glomerulosclerosis / glomerulonephritis / nephrotic syndrome | 41 |
Autosomal dominant polycystic kidney disease | 402 | Cystinuria | 30 |
Tubulopathy or other fluid / electrolyte imbalance (Gitelman, Bartter, renal tubular acidosis, Dent / Lowe) | 212 | Conn syndrome | 15 |
Unspecified cystic kidney disease / HNF1b nephropathy (renal cysts and diabetes symdrome) / autosomal recessive polycystic kidney disease) | 85 | Congenital anomalies of the kidney and urinary tract or reflux disease | 12 |
Genetics consult only | 68 | Familial hypertensive nephropathy | 9 |
Alport syndrome / thin basement membrane / haematuria | 63 | Mitochondrial nephropathy | 7 |
Uromodulin-associated nephropathy / autosomal dominant tubulointerstitial kidney disease | 50 | Tuberous sclerosis | 6 |
At-risk family member – found to be unaffected | 47 | Other (Liddle, oral–facial–digital syndrome branchio–oto–renal syndrome, familial hypocalciuric hypercalcaemia) | 14 |