Monogenic and Syndromic Obesity Precision Panel
The heritability of obesity is estimated between 40-70%, but the genetics of obesity for most individuals is complex and involves the interaction of multiple genes with the environment.
Hyperlipidemia Precision Panel
Hyperlipidemia is a set of metabolic disorders that can be genetic or acquired that are characterized by excess lipids in the blood which can include cholesterol and/or triglycerides.
MODY and Neonatal Diabetes Precision Panel
Maturity-onset diabetes of the young (MODY) and Neonatal Diabetes Mellitus are a heterogeneous group of inherited monogenic and polygenic disorders that are present during adolescence or young adulthood and affect an individual’s blood sugar level due to beta cell dysfunction.
Disorders of Sex Development Precision Panel
Disorders of Sex Development (DSD), formerly termed intersex conditions, occur when there is a discrepancy between the appearance of the genitalia and the genetic makeup of an individual.
Hereditary Pancreatitis Precision Panel
Pancreatitis is a condition that occurs when the pancreas becomes inflamed leading to a state of systemic inflammation.
Congenital Adrenal Hyperplasia Precision Panel
Congenital Adrenal Hyperplasia (CAH) is a group of diseases that are associated with variants or mutations in the genes that are involved in hormone production.