Sponsored diagnostic testing programs for Monogenic Common Variable Immune Deficiency (CVID)
Monogenic Common Variable Immune Deficiency (CVID) is a primary immunodeficiency caused by single-gene defects that impair antibody production. It leads to recurrent infections, reduced immunoglobulin levels, and may be associated with autoimmunity, gastrointestinal issues, or chronic lung disease.
2 programs found for Monogenic Common Variable Immune Deficiency (CVID)
Invitae Unlock™ Immunology provides clinicians with a comprehensive gene panel to evaluate patients with suspected primary immunodeficiency or immune-regulatory disorders. This no-charge program supports diagnostic clarification, aids in variant-guided care decisions, and can inform family cascade testing when appropriate.
Invitae Unlock Immunology offers sponsored access to the Inborn Errors of Immunity and Cytopenias Panel, Invitae’s most comprehensive assay for evaluating inherited immune disorders and cytopenias. The panel includes genes tied to combined immunodeficiencies, immune dysregulation, and bone marrow failure, supporting clearer diagnosis and management. U.S. providers may order for eligible patients.
