Genetic and specialty testing programs for liver and hepatobiliary conditions
Hepatology conditions+Hepatology includes sponsored testing programs that offer no-cost or low-cost access to genetic and specialty testing for hereditary liver disorders, cholestatic diseases, metabolic liver conditions, and other hepatobiliary issues. These programs help identify underlying causes of liver dysfunction, support earlier and more accurate diagnosis, and connect patients and clinicians with sponsored testing options focused on comprehensive liver health evaluation.
3 programs found in Hepatology
This program offers no-charge comprehensive genetic testing for patients in the US or Canada with suspected inherited cholestatic liver disease. The Invitae Cholestasis Panel evaluates key genes associated with PFIC, ALGS, and other cholestatic disorders. Clinicians receive actionable results, and patients are eligible for complimentary post-test genetic counseling.
This program provides no-cost access to genetic testing for U.S. patients with confirmed or suspected PBD-ZSD. The panel evaluates core PEX genes associated with peroxisome biogenesis disorders and supports diagnosis, management, and assessment of disease severity. Providers assess eligibility, coordinate specimen collection and shipping, and review both genetic and reflex biochemical results.
This program provides complimentary genetic testing for U.S. patients with current or historical cholestasis, unexplained chronic liver disease, or clinical features suggestive of inherited bile acid or hepatobiliary disorders. The panel includes key cholestasis and PFIC-related genes and supports diagnosis, management, and familial variant clarification. Eligibility excludes extrahepatic causes and TPN-associated cholestasis.
