Familial Essential Thrombocythemia

Sponsored diagnostic testing programs for Familial Essential Thrombocythemia

Familial Essential Thrombocythemia is an inherited bone marrow disorder marked by persistently elevated platelet counts due to genetic variants affecting blood cell regulation. Individuals may be asymptomatic or experience headaches, microvascular symptoms, or an increased risk of clotting or bleeding.

1 program found for Familial Essential Thrombocythemia

Programs

1 program
Invitae Unlock™

Invitae Inborn Errors of Immunity and Cytopenias Panel

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.

Immunology