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DNA - carrier status

Reveal disease traits potentially passed to your children like cystic fibrosis, Gaucher disease, Tay-Sachs and hearing loss. See the complete list below:

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  • 3-Methylcrotonyl-CoA carboxylase deficiency
  • Acrodermatitis enteropathica
  • Alpha-1 antitrypsin deficiency
  • Amyotrophic lateral sclerosis
  • Argininosuccinate lyase deficiency (Caucasian only)
  • Autoimmune polyglandular syndrome, type I
  • Bartter syndrome, type 4A
  • Beta-ketothiolase deficiency
  • Beta-thalassemia
  • Biotinidase deficiency
  • Bloom syndrome
  • Canavan disease
  • Carnitine deficiency, primary systemic
  • Cerebrotendinous xanthomatosis
  • Citrullinemia, type I
  • Corticosterone methyl oxidase deficiency
  • Crigler-Najjar syndrome
  • Cystic fibrosis
  • Diabetes, permanent neonatal
  • Dihydropyrimidine dehydrogenase deficiency
  • Dubin-Johnson syndrome
  • Ehlers-Danlos syndrome, dermatosparaxis
  • Ehlers-Danlos syndrome, hypermobility
  • Ehlers-Danlos syndrome, kyphoscoliotic
  • Ethylmalonic aciduria
  • Factor XI deficiency
  • Familial dysautonomia
  • Familial Mediterranean fever
  • Fanconi anemia
  • Galactokinase deficiency
  • Galactosemia
  • Gaucher disease
  • Glutaric acidemia, type 1
  • Glycogen storage disease, type 1A
  • GM1-gangliosidosis
  • Hearing loss, DFNB1 and DFNB9 nonsyndromic
  • Hearing loss, DFNB59 nonsyndromic
  • Hemochromatosis
  • Hemoglobin C
  • Hemoglobin E
  • HMG-CoA lyase deficiency
  • Homocystinuria, cblE type
  • Homocystinuria, classic
  • Hurler syndrome
  • Krabbe disease
  • Lipoprotein lipase deficiency, familial
  • Maple syrup urine disease
  • Medium-chain acyl-CoA dehydrogenase deficiency
  • Methylmalonic acidemia
  • Mucolipidosis II
  • Mucolipidosis III
  • Mucolipidosis IV
  • Multiple carboxylase deficiency
  • Nephrotic syndrome, steroid-resistant
  • Niemann-Pick disease
  • Phenylketonuria
  • Polycystic kidney disease
  • Pompe disease
  • Prekallikrein deficiency
  • Propionic acidemia
  • Prothrombin deficiency
  • Rh-null syndrome
  • Rickets, pseudovitamin D-deficiency
  • Sandhoff disease
  • Short-chain acyl-CoA dehydrogenase deficiency
  • Sick sinus syndrome
  • Sickle cell disease
  • Spherocytosis, hereditary
  • Tay-Sachs disease
  • Tay-Sachs pseudodeficiency
  • Thrombocytopenia, congenital amegakaryocytic
  • Tyrosinemia
  • Very long-chain acyl-CoA dehydrogenase deficiency
  • Von Willebrand disease, type 2 Normandy
  • Von Willebrand disease, type 3

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