Hepatic veno-occlusive disease-immunodeficiency syndrome

Hepatic veno-occlusive disease-immunodeficiency syndrome is characterized by the association of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease.

Also known as: VODI syndrome, VODI, familial veno-occlusive disease with immunodeficiency, hepatic veno-occlusive disease with immunodeficiency, hepatic venoocclusive disease with immunodeficiency, veno-occlusive disease and immunodeficiency syndrome

41 clinical trials for this condition and its sub-types, 0 tagged with Hepatic veno-occlusive disease-immunodeficiency syndrome itself.