NxGen Super Panel

The NxGen Super Panel is one of the world's largest, most precise, and thorough tests for detecting genetic markers for 113 of the most common genetic diseases that may affect pregnancy and future child development.

NxGen Super Panel

What Is It?

The NxGen Super Panel screens for common genetic conditions across multiple ethnicities, such as cystic fibrosis, sickle cell anemia, and Tay-Sachs. It also screens for conditions that are more rare such as Krabbe and Zellweger syndrome. While many individuals have not heard of the conditions listed on the Super Panel, these genetic conditions can cause a variety of health concerns, including intellectual delay or developmental delays that may necessitate life-long management.

To learn more about the Super Panel, download the brochure. The NxGen Super Panel can help determine if you are a carrier for the following genetic diseases:

  • 3-Phosphoglycerate Dehydrogenase Deficiency
  • ABCC8-Related Hyperinsulinism
  • Abetalipoproteinemia
  • Achromatopsia
  • Alkaptonuria
  • Alpha Thalassemia
  • Alpha-Mannosidosis
  • Alport Syndrome, Autosomal Recessive
  • Andermann Syndrome
  • Arthrogryposis, Mental Retardation, and Seizures (AMRS)
  • Aspartylglucosaminuria
  • Ataxia With Vitamin E Deficiency
  • Ataxia-Telangiectasia
  • Autosomal Recessive Polycystic Kidney Disease
  • Bardet-Biedl Syndrome, BBS1-Related
  • Bardet-Biedl Syndrome, BBS10-Related
  • Beta Thalassemia
  • Biotinidase Deficiency
  • Bloom Syndrome
  • Canavan Disease
  • Carnitine Palmitoyltransferase IA Deficiency
  • Carnitine Palmitoyltransferase II Deficiency
  • Cartilage-Hair Hypoplasia
  • Choroideremia
  • Classic Citrullinemia
  • CLN3-Related Neuronal Ceroid Lipofuscinosis
  • CLN5-Related Neuronal Ceroid Lipofuscinosis
  • Cohen Syndrome
  • Congenital Amegakaryocytic Thrombocytopenia
  • Congenital Disorder of Glycosylation Type Ia
  • Congenital Disorder of Glycosylation Type Ib
  • Congenital Finnish Nephrosis
  • Costeff Optic Atrophy Syndrome
  • Cystic Fibrosis
  • Cystinosis
  • D-Bifunctional Protein Deficiency
  • Dihydrolipoamide Dehydrogenase Deficiency
  • Dyskeratosis Congenita, Autosomal Recessive
  • Ehlers-Danlos, Type VIIC
  • Factor XI Deficiency
  • Familial Dysautonomia
  • Familial Mediterranean Fever
  • Fanconi Anemia Type C
  • Fragile X
  • Galactosemia
  • Gaucher Disease
  • GJB2-related DFNB1 Nonsyndromic Hearing Loss and Deafness
  • Glucose-6-Phosphate Dehydrogenase Deficiency
  • Glutaric Acidemia Type 1
  • Glycogen Storage Disease Type Ia
  • Glycogen Storage Disease Type Ib
  • Glycogen Storage Disease Type III
  • Glycogen Storage Disease Type V
  • GRACILE Syndrome
  • Hereditary Fructose Intolerance
  • Hereditary Thymine-Uraciluria
  • Homocystinuria
  • Hurler Syndrome
  • Hypophosphatasia, Autosomal Recessive
  • Inclusion Body Myopathy 2
  • Isovaleric Acidemia
  • Joubert Syndrome 2
  • Krabbe Disease
  • LAMA3-Related Junctional Epidermolysis Bullosa
  • LAMB3-Related Junctional Epidermolysis Bullosa
  • LAMC2-Related Junctional Epidermolysis Bullosa
  • Limb-Girdle Muscular Dystrophy Type 2D
  • Limb-Girdle Muscular Dystrophy Type 2E
  • Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
  • Maple Syrup Urine Disease Type I
  • Medium Chain Acyl-CoA Dehydrogenase Deficiency
  • Megalencephalic Leukoencephalopathy With Subcortical Cysts
  • Metachromatic Leukodystrophy
  • Mucolipidosis IV
  • Multiple Sulphatase deficiency
  • Muscle-Eye-Brain Disease
  • NEB-Related Nemaline Myopathy
  • Niemann-Pick Disease Type C
  • Niemann-Pick Disease, SMPD1-Associated
  • Nijmegen Breakage Syndrome
  • Northern Epilepsy
  • Pendred Syndrome
  • PEX1-Related Zellweger Syndrome Spectrum
  • Phenylalanine Hydroxylase Deficiency
  • Polyglandular Autoimmune Syndrome Type 1
  • Pompe Disease
  • PPT1-Related Neuronal Ceroid Lipofuscinosis
  • Primary Carnitine Deficiency
  • Primary Hyperoxaluria Type 1
  • Primary Hyperoxaluria Type 2
  • PROP1-Related Combined Pituitary Hormone Deficiency
  • Pycnodysostosis
  • Retinitis Pigmentosa 59
  • Rhizomelic Chondrodysplasia Punctata Type 1
  • Salla Disease
  • Segawa Syndrome
  • Short Chain Acyl-CoA Dehydrogenase Deficiency
  • Sickle Cell Anemia
  • Sjogren-Larsson Syndrome
  • Smith-Lemli-Opitz Syndrome
  • Spinal Muscular Atrophy
  • Steroid-Resistant Nephrotic Syndrome
  • Sulfate Transporter-Related Osteochondrodysplasia
  • Tay-Sachs Disease
  • TPP1-Related Neuronal Ceroid Lipofuscinosis
  • Tyrosinemia Type I
  • Usher Syndrome Type 1F
  • Usher Syndrome Type 3
  • Very Long Chain Acyl-CoA Dehydrogenase Deficiency
  • Walker-Warburg
  • Wilson Disease
  • X-Linked Juvenile Retinoschisis

Who Should Take It?

• All individuals of child bearing age, regardless of gender.
• All individuals with a family history of genetic disorders.
• All individuals with partners who are carriers of genetic disorders.
• Those considering in vitro fertilization.
• Pregnant women.

Why NxGen?

When testing, our laboratory analyzes all of the coding DNA in a gene to determine if any disease-causing pathogenic variants are present. By sequencing all of the coding DNA in a gene, instead of just a portion, we are able to offer the most accurate genetic testing available, regardless of your ethnicity. The majority of laboratories are only sequencing a portion of the gene, leaving room for error with missed pathogenic variants, especially when testing a variety of ethnicities. By sequencing the entire gene, NxGen MDx testing eliminates the doubt in a negative result and drastically reduces the residual risk, regardless of ethnicity.

Talk to a Genetic Counselor

As a NxGen client, you'll have access to personal genetic counselors who can help explain the results of your screens and provide insight on how to move forward. To schedule a personal conference to discuss your screen results, call (855) 776-9436. or click the link below.

Discuss Your Screening Results

Connect With Our Customer Care Center

Get answers to all your questions related to billing, insurance coverage, the status of your screening results, and more by calling us at (855) 776-9436 or clicking the link below.

Connect With Our  Customer Care Center