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ReadyGen screens for
more than 200 conditions

ReadyGen is a simple, at-home test that gives early insight into your child's health. This test only includes conditions that may be treated with medication, dietary modification, or other therapies, so proactive steps can be taken with a pediatrician to care for your child’s health.

Every order also includes additional pharmacogenomic analysis of your child’s response or sensitivity to more than 40 medications.

  • Alpha Thalassemia
  • Beta Thalassemia
  • Congenital Amegakaryocytic Thrombocytopenia
  • Dyskeratosis Congenita
  • Factor 9 Deficiency (Hemophilia B)
  • Fanconi Anemia
  • Hemolytic Anemia G6PD-related
  • Sickle Cell Disease
  • Spherocytosis Type 1
  • Spherocytosis Type 5
  • Retinoblastoma
  • Wilms Tumor
  • Adenosine deaminase deficiency
  • Congenital neutropenia
  • Chronic granulomatous disease CYAB-related
  • Chronic granulomatous disease CYBB-related
  • Immunodeficiency 18
  • Immunodeficiency 19
  • Omenn Syndrome DCLRE1C-related
  • Omenn Syndrome RAG1-related
  • Omenn Syndrome RAG2-related
  • Severe Combined Immunodeficiency Athabaskan Type
  • Severe Combined Immunodeficiency IL7R-related
  • Severe Combined Immunodeficiency JAK3-related
  • Severe Combined Immunodeficiency PTPRC-related
  • X-linked Severe Combined Immunodeficiency
  • 3-Beta-Hydroxysteroid Dehydrogenase Type II Deficiency
  • 3-Methylcrotonyl-CoA Carboxylase Deficiency MCCC1-related
  • 3-Methylcrotonyl-CoA Carboxylase Deficiency MCCC2-related
  • 3-Phosphoglycerate Dehydrogenase Deficiency
  • 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
  • Abetalipoproteinemia
  • Acrodermatitis Enteropathica
  • Argininemia
  • Argininosuccinic Aciduria
  • Barth Syndrome
  • Beta-Ketothiolase Deficiency
  • BH4-Deficient Hyperphenylalaninemia C
  • BH4-Deficient Hyperphenylalaninemia D
  • Biotinidase Deficiency
  • Carbamoylphosphate Synthetase I Deficiency
  • Carnitine Acylcarnitine Translocase Deficiency
  • Carnitine Palmitoyltransferase IA Deficiency
  • Carnitine Palmitoyltransferase II Deficiency
  • Central Hypothyroidism and Testicular Enlargement
  • Cerebral Creatine Deficiency Syndrome 2
  • Cerebral Creatine Deficiency Syndrome 3
  • Citrin Deficiency
  • Citrullinemia Type I
  • Combined Pituitary Hormone Deficiency 1
  • Combined Pituitary Hormone Deficiency 2
  • Combined Pituitary Hormone Deficiency 3
  • Congenital Adrenal Hyperplasia due to 11-beta-hydroxylase deficiency
  • Congenital Disorder of Glycosylation Type Ib
  • Congenital Hypothyroidism due to Dyshormonogenesis or Hypoplasia
  • Congenital Nongoitrous Hypothyroidism 1/Nonautoimmune Hyperthyroidism
  • Congenital Nongoitrous Hypothyroidism 4
  • Congenital Nongoitrous Hypothyroidism 6
  • Corticosterone Methyloxidase Deficiency
  • Cystinosis
  • Dopa-Responsive Dystonia/BH4-Deficient Hyperphenylalaninemia B
  • Ethylmalonic Encephalopathy
  • Familial Hypercholesterolemia
  • Familial Hyperinsulinemia ABCC8-related
  • Familial Hyperinsulinemia KCNJ11-related
  • Familial Hyperinsulinemic Hypoglycemia 4/3-Hydroxyacyl CoA Dehydrogenase Deficiency
  • Fabry Disease
  • Fructose 1,6 Bisphosphotase Deficiency
  • Galactokinase Deficiency
  • Galactose Epimerase Deficiency
  • Galactosemia
  • Gaucher Disease
  • Glutathione Synthetase Deficiency
  • Glutaric Acidemia Type I
  • Glutaric Acidemia Type IIa
  • Glutaric Acidemia Type IIb
  • Glutaric Acidemia Type IIc
  • Glycogen Storage Disease Type 0
  • Glycogen Storage Disease Type Ia
  • Glycogen Storage Disease Type II (Pompe DIsease)
  • Glycogen Storage Disease Type III
  • Glycogen Storage Disease Type VI
  • Glycogen Storage Disease Type IXb
  • Hereditary Fructose Intolerance
  • HMG-CoA Lyase Deficiency
  • HMG-CoA Synthetase Deficiency
  • Holocarboxylase Synthetase Deficiency
  • Homocystinuria
  • Homocystinuria Cobalamin E Type
  • Homocystinuria-Megaloblastic Anemia Cobalamin G Type
  • Hunter syndrome (MPS-II)
  • Hurler syndrome (MPS-IH)
  • Hyperinsulinemia-Hyperammonemia Syndrome
  • Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome
  • Generalized Thyrotropin-Releasing Hormone Resistance
  • Isovaleric Acidemia
  • Krabbe Disease
  • Lipoamide Dehydrogenase Deficiency
  • Lipoid Adrenal Hyperplasia
  • Lipoprotein Lipase Deficiency
  • Long Chain 3-Hydroxyacyl CoA Dehydrogenase Deficiency
  • Lysinuric protein intolerance
  • Malonyl-CoA Decarboxylase Deficiency
  • Maple Syrup Urine Disease Type 1A
  • Maple Syrup Urine Disease Type 1B
  • Maple Syrup Urine Disease Type 2
  • Mannosidosis
  • Maroteaux-Lamy Syndrome (MPS-VI)
  • Medium Chain Acyl-CoA Dehydrogenase Deficiency
  • Metachromatic Leukodystrophy
  • Methionine adenosyltransferase I/III deficiency
  • Methylmalonic Acidemia MMAA-related
  • Methylmalonic Acidemia MMAB-related
  • Methylmalonic Acidemia MUT-related
  • Methylmalonic Aciduria and Homocystinuria Cobalamin C Type
  • Methylmalonic Aciduria and Homocystinuria Cobalamin D Type
  • Methylmalonic Aciduria and Homocystinuria Cobalamin F Type
  • Methylmalonyl-CoA Epimerase Deficiency
  • Mitochondrial Trifunctional Protein Deficiency
  • Morquio Syndrome (MPS-IVa)
  • Mucolipidosis II (I-cell Disease)
  • N-Acetylglutamate Synthase Deficiency
  • Neonatal Hyperparathyroidism/Autosomal Dominant Hypocalcemia
  • Neuronal Ceroid Lipofuscinosis (Batten Disease)
  • Niemann-Pick Syndrome
  • Ornithine Transcarbomylase Deficiency
  • Permanent Neonatal Diabetes Mellitus INS-related
  • Phenylalanine Hydroxylase Deficiency (Phenylketonuria)
  • Primary Carnitine Deficiency
  • Propionic Acidemia PCCA-related
  • Propionic Acidemia PCCB-related
  • Pyridoxamine 5’-Oxidase Deficiency
  • Sanfilippo Syndrome (MPS-III)
  • Scheie Syndrome (MPS-IS)
  • Sepiapterin Reductase Deficiency
  • Tay Sachs Disease
  • Thyroid Dyshormonogenesis 1
  • Thyroid Dyshormonogenesis 2A
  • Thyroid Dyshormonogenesis 3
  • Thyroid Dyshormonogenesis 4
  • Thyroid Dyshormonogenesis 5
  • Thyroid Dyshormonogenesis 6
  • Tyrosinemia Type I
  • Tyrosinemia Type II
  • Tyrosinemia Type III
  • Very Long Chain Acyl-CoA Dehydrogenase Deficiency
  • Wolman Syndrome/Cholesteryl Ester Storage Disease
  • X-Linked Adrenoleukodystrophy
  • Acute Infantile Liver Failure
  • Alagille Syndrome
  • Alport Syndrome COL4A3 related
  • Alport Syndrome COL4A4 related
  • Alport Syndrome COL4A5 related
  • Crigler-Najjar Syndrome 1
  • Crigler-Najjar Syndrome 2
  • Congenital Bile Acid Synthesis Defect AKR1D1-related
  • Congenital Bile Acid Synthesis Defect HSD3B7-related
  • Distal Renal Tubular Acidosis
  • Gilbert syndrome
  • Nephrogenic Diabetes Insipidus Type II
  • Nephrogenic Diabetes Insipidus
  • Nephrogenic Syndrome of Inappropriate Antidiuresis
  • Primary Hyperoxaluria Type 1
  • Primary Hyperoxaluria Type 2
  • Primary Hyperoxaluria Type 3
  • Ataxia with Isolated Vitamin E Deficiency
  • Cerebrotendinous Xanthomatosis
  • Dravet Syndrome
  • Early Infantile Epilectic Encephalopathy 7/Benign Neonatal Seizures 1
  • Early Infantile Epilectic Encephalopathy 11/Benign Neonatal Seizures 3
  • Early Infantile Epilectic Encephalopathy 13/Benign Neonatal Seizures 5
  • Familial Infantile Convulsions with Paroxysmal Choreoathetosis
  • Glucose Transporter 1 Deficiency Syndrome
  • Neurodegeneration due to Cerebral Folate Transport Deficiency
  • Pyridoxine-Dependent Epilepsy
  • Segawa Syndrome
  • Spinal Muscular Atrophy
  • Cystic Fibrosis
  • Tetralogy of Fallot
  • Hypophosphatasia
  • Marfan syndrome
  • Ornithine Aminotransferase Deficiency
  • Osteopetrosis I

Questions? Visit FAQs or call 1-888-489-0035

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