Achondroplasia
Assesses the hereditary risk of achondroplasia, a common cause for dwarfism
Ankylosing spondylitis
Assesses the hereditary risk of ankylosing spondylitis, a degenerative arthritis that affects the spine and joints
Azoospermia
Assesses the hereditary risk of Azoospermia, a condition that affects the sperm count in a man's ejaculate
Blood cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Breast cancer
Detects all the pathogenic mutations in BRCA1 and BRCA2 that commonly increases the risk for hereditary breast and ovarian cancer
Calpainopathy
Detects CAPN3 gene mutation which causes calpainopathy
Cervical cancer
Designed for people who are vaccinated against HPV
Colorectal cancer
Assesses120 most common hereditary cancer diseases.
Cystic fibrosis
Assesses the hereditary risk of cystic fibrosis, a disease that can damage the respiratory and digestive system
Down’s syndrome
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
Duchenne and Becker muscular dystrophy
Assesses DMD gene condition which relates to Duchenne and Becker muscular dystrophy
Edward syndrome
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
Endocrine cancer
Assesses120 most common hereditary cancer diseases.
Eye infection in new-born baby
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Fragile X syndrome
Assesses the hereditary risk of fragile X syndrome, a condition that leads to mental retardation
Head & Neck cancer
Assesses120 most common hereditary cancer diseases.
Heart conditions
Detects 81 inherited Cardiac Diseases & covers 255 Genes associated with Inherited Cardiac Diseases
Infertility
Assesses the hereditary risk of Azoospermia, a condition that affects the sperm count in a man's ejaculate
Kidney cancer
Assesses120 most common hereditary cancer diseases.
Lung cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Neuroblastoma
Assesses120 most common hereditary cancer diseases.
Neurofibromatosis
Assesses120 most common hereditary cancer diseases.
Ovarian cancer
Detects all the pathogenic mutations in BRCA1 and BRCA2 that commonly increases the risk for hereditary breast and ovarian cancer
Pancreatic cancer
Assesses120 most common hereditary cancer diseases.
Paraganglimo cancer
Assesses120 most common hereditary cancer diseases.
Patau syndrome
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
Pelvic Inflammatory Disease
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Premature labour
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Prostate cancer
Professional protection of your health
Rare inherited diseases
The premium service which screens for 2700+ genes, 900+diseases in one single test
Retinoblastoma
Assesses120 most common hereditary cancer diseases.
Sexually transmitted disease (STD)
Identifies 33 known HPV types which may lead to cervical cancer and genital warts. (Companion testing with Pap test optional)
Skin cancer
Assesses120 most common hereditary cancer diseases.
Spinal muscular atrophy
Assesses the hereditary risk of spinal muscular atrophy, a neuromuscular disorder that leads to muscle weakness
Still-births
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Stomach cancer
Assesses120 most common hereditary cancer diseases.
Thrombophilia
Assesses the hereditary risk of thrombophilia, a condition associated with an increased risk of pregnancy loss
Trisomy X, Y syndrome
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
α thalassemia
Assesses the hereditary risk of α-thalassemia
β thalassemia
Assesses the hereditary risk of β-thalassemia
