Services Offered

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This panel investigates drug sensitivity and the way body react to various medications. This test determines which medications are most appropriate based on genetic build up of individuals.    

This panel investigates genetic variances related to autoimmune disorders, sarcoidosis, and inborn immunodeficiency. 

This panel identifies the risk of genetic factors for various cancers such as breast cancer, ovarian cancer, prostate cancer, and others that run in a family. 

Maturity Onset Diabetic of the Young (MODY) is a group of disorders characterized by type I or type II diabetes that start at in the initial decades of life. This panel tests for genes involved in this disorder. 

Investigates the risk of early onset dementia and other neurological disorders in families

DM is a group of metabolic disorders characterized by a high blood sugar level over a prolonged period of time . This panel tests for genes involved in this disorder.

This panel is designed by and genes are carefully selected by expert pulmonologist and Intensive Care Unit Physician, Professor Mirsaeidi, from the University of Miami, Miller School of Medicine. The genes and mutations in this panel, investigate genetic susceptibility to COPD, Asthma, Interstitial Lung Disease, Cystic Fibrosis, Pneumonia, Sarcoidosis, and Mycobacterial Disease.  

This panel checks for the likelihood of developing various retinopathies, leber congenital amaurosis, cataract, and glaucoma. Some patients with retinopathies may receive gene therapy based on the type of mutation identified. 

Examines 110 genes related to Autism 

Tests all coding exons to identify causes of unidentified genetic conditions.

This panel investigates mutations as well as deletions and duplications in two genes related to breast cancer. 

This panel investigates genes involved in hearing impairments. Hearing impairment can be deafness or partial hearing impairments. 

Identifies if a healthy person is a carrier of genetic mutation and consequences such as disease later in life and the ability to pass to the next generation

This panel investigates the possibility and causes of metabolic diseases such as early infantile diabetes, liver enzyme processing problems, and maple syrup urine disorder (MSUD). 

Used to determine the susceptibility of various cardiomyopathy and other cardiac related disorders. 

This panel investigates the cause of various skin disorders such as atopy, psoriasis, butterfly disease, and eczema. 

This panel investigates rare multi-systemic congenital or infantile disorders.

This panel investigates hereditary causes of intellectual disabilities in children and young adults. 

Explores genetic causes of any hematological disorders such as Sickle-cell anemia and coagulopathies (bleeding disorders). 

This panel investigates the cause of diseases related to mitochondrial chain reaction. Mitochondria are organelles that generate energy for all cellular activities. 

This panel investigates disorders related to muscle and the neuromuscular system such as limb-girdle muscular dystrophy.  

This important prenatal test recommended for all pregnant ladies at 10 weeks of gestations. The NIPT test determining the risk that the fetus will be born with certain chromosomal abnormalities, such as Trisomy 21 (Down Syndrome), Trisomy 18, and Trisomy 13. 

Used to determine the genetic/blood relationship between 2 or 3 people 

COVID-19 RT PCR test suitable for traveling and for exposure. 99% accuracy for positive results and 97% accuracy for negative results

Walk-in accepted