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Nephrology, Endocrinology, and Electrolytes

Nephrology, Endocrinology, and Electrolytes

  • 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)

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