Hypoplasminogenemia

Disease Export to PDF
Name:
Hypoplasminogenemia
Description:
A rare multi-system disease characterized by markedly impaired extracellular fibrinolysis leading to the formation of ligneous (fibrin-rich) pseudomembranes on mucosae.
ORPHAcode:
722
Synonyms:
Plasminogen deficiency type 1
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14