All Conditions We Test For in the Carrier Status Report:

• 3-Methylcrotonyl-CoA carboxylase deficiency
• Acrodermatitis enteropathica
• Alpha-1 antitrypsin deficiency
• Amyotrophic lateral sclerosis
• Argininosuccinate lyase deficiency
• 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
• MTHFR deficiency
• 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