• Congenital adrenal hyperplasia, rare causes (DxOme Not Available) includes 4 Gene(s)

• Diabetes, neonatal (DxOme Not Available) includes 5 Gene(s)

• Autosomal dominant tubulointerstitial kidney disease (ADTKD) includes 3 Gene(s)

• Alport syndrome / Thin basement membrane nephropathy includes 4 Gene(s)

• Branchiootorenal / Brachiootic syndrome (BOR and BOS) includes 3 Gene(s)

• Congenital anomalies of the kidney and urinary tract (CAKUT) includes 30 Gene(s)

• Renal disease and electrolytes - entire panel includes 114 Gene(s)

• Maturity-onset diabetes of the young (MODY) (DxOme Not Available) includes 15 Gene(s)

• Urethra malformations includes 9 Gene(s)

• Fraser syndrome includes 3 Gene(s)

• Focal segmental glomerulosclerosis (FSGS) includes 13 Gene(s)

• Focal segmental glomerulosclerosis (FSGS) - core panel includes 8 Gene(s)

• Hyperkalemia / Pseudohypoaldosteronism includes 4 Gene(s)

• Hypokalemia and Gitelman / Bartter syndrome includes 8 Gene(s)

• Hypoplasia of the kidney and renal agenesis includes 8 Gene(s)

• Nephrotic syndrome includes 26 Gene(s)

• Nephrotic syndrome - core panel includes 5 Gene(s)

• Polycystic liver disease includes 6 Gene(s)

• Polycystic kidney disease includes 16 Gene(s)

• Polycystic kidney disease - core panel includes 3 Gene(s)

• Renal calculi includes 11 Gene(s)

• Renal tubular dysgenesis includes 4 Gene(s)