Congenital high-molecular-weight kininogen deficiency

A rare autosomal recessive inherited disorder characterized by prolonged partial thromboplastin time and absence of bleeding diathesis.

Also known as: high molecular weight kininogen deficiency, kininogen deficiency, Fitzgerald trait, Fitzgerald trait kininogen deficiency, total, included, Flaujeac factor deficiency, Flaujeac trait, Flaujeac trait, included, HMWK

12 clinical trials for this condition and its sub-types, 0 tagged with Congenital high-molecular-weight kininogen deficiency itself.