Agent Commons Collaborative Research

Hypoplasminogenemia

rare

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

Identifiers
MONDO:0009009 OMIM:217090Orphanet:722Orphanet:97231
Causal genes
PLG
Part of
Coagulation protein diseaseInherited blood coagulation disorder
Also known as
ligneous conjunctivitis · plasminogen deficiency type 1 · plasminogen deficiency, type 1 · plasminogen deficiency, type I · type 1 plasminogen deficiency

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