The Carrier Screening 18 test is a genetic test that screens for 18 specific genetic diseases.
1-2. Alpha Thalassemia
3. Beta Thalassemia
4. Galactosemia
5. Phenylketonuria (PKU)
6. G6PD Deficiency
7. Citrin Deficiency
8. Steroid 5-alpha-reductase Deficiency
9. Glycogen Storage Disease Type II (Pompe)
10. Wilson Disease
11. Cystic Fibrosis
12. Tay–Sachs Disease
13. Glutaric aciduria type II
14. Fabry Disease
15. Congenital adrenal hyperplasia
16. Congenital hypothyroidism
17. Biotinidase deficiency
18. Spinal Muscular Atrophy

