• Pseudohypoparathyroidism GNAS - methylation analysis includes 1 Gene(s)

• Congenital adrenal hyperplasia, rare causes (DxOme Not Available) includes 5 Gene(s)

• Monogenetic arterial Hypertension includes 19 Gene(s)

• Diabetes, neonatal (DxOme Not Available) includes 6 Gene(s)

• Hyperinsulinism includes 17 Gene(s)

• Ciliopathies includes 184 Gene(s)

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

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

• Branchio-Oto-Renal /-Oculofacial Syndrom (BOR / BOS / BOFS) includes 4 Gene(s)

• Congenital anomalies of the kidney and urinary tract (CAKUT) includes 64 Gene(s)

• Renal disease and electrolytes - entire panel includes 250 Gene(s)

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

• Familial Hyperaldosteronism Type I - IV incl. PASNA includes 6 Gene(s)

• Fraser syndrome includes 3 Gene(s)

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

• Hypercalcemia includes 15 Gene(s)

• Hyperkalemia / (Pseudo)hypoaldosteronism includes 9 Gene(s)

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

• Nephronophthisis includes 21 Gene(s)

• Proteinuric renal disease includes 61 Gene(s)

• Polycystic liver disease includes 7 Gene(s)

• Polycystic kidney disease includes 10 Gene(s)

• Polycystic kidney disease - PKD1, PKD2 includes 2 Gene(s)

• Resistance to Thyroid Hormone Action (incl. syndromic causes) includes 5 Gene(s)

• Renal calculi and nephrocalcinosis includes 35 Gene(s)

• Renal tubular dysgenesis includes 4 Gene(s)

• Non-syndromic Differences of Sex Development (DSD) includes 31 Gene(s)