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Hypoplasminogenemia

MONDO:0009009

A rare multi-system disease characterized by markedly impaired extracellular fibrinolysis leading to the formation of ligneous (fibrin-rich) pseudomembranes on mucosae.

Also known as: hypoplasminogenemia, plasminogen deficiency type 1, plasminogen deficiency, type 1, plasminogen deficiency, type I, type 1 plasminogen deficiency, ligneous conjunctivitis

6 clinical trials for this condition and its sub-types, 1 tagged with Hypoplasminogenemia itself.

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Part of

↑ Inherited blood coagulation disorder (323) ↑ Coagulation protein disease (274)

Including sub-types (6) Tagged with Hypoplasminogenemia (1)

Trials to join now! 1

Scientists launch global effort to unlock mysteries of rare blood disorder

Knowledge-focused Recruiting now

This study is for people with plasminogen deficiency (a rare blood disorder) and their close family members. Researchers will collect medical history and blood samples over several years to better understand how the disease develops and varies between people. No new treatments ar…

Sponsor: Indiana Hemophilia &Thrombosis Center, Inc. • Aim: Knowledge-focused

Last updated Jun 27, 2026 13:03 UTC

Hypoplasminogenemia

Where it sits in the disease tree

Scientists launch global effort to unlock mysteries of rare blood disorder