If you have a health condition that is difficult to diagnose, or a family history of medical problems, your doctor might recommend exome sequencing for additional clues.
Neurogenetics uses genome sequencing to understand the cause of brain and nerve disorders, such as Alzheimer's, ALS and many others.
Whole genome sequencing can search a person's entire DNA for genetic variants that may be linked to a disease or condition.
Lynch syndrome is an inherited genetic disorder linked to an increased risk of developing cancer, often at a younger age in life—especially colorectal cancer, and, for women, endometrial cancer.
Cancers of the breast and ovaries caused by genetic mutations.
Genetic evaluation and counseling involves a consultation that provides an individual's risk of acquiring inheritable conditions. Learn more about this service.
A genetic disorder of blood vessels that affects people of all ages and backgrounds.
Huntington’s disease is a rare, inherited neurodegenerative condition that slowly and permanently robs a person’s physical and mental health.
A rare, fast-growing type of cancer that begins in the brain and/or spinal cord.
Cardiomyopathy is a condition in which the heart muscle has difficulty pumping blood. Learn about symptoms and treatment.