has characteristic has characteristic has material basis in germline mutation in PLG coagulation protein disease chronic conjunctivitis eye disorder conjunctival disorder hypoplasminogenemia https://github.com/monarch-initiative/mondo/issues/7100 https://github.com/monarch-initiative/mondo/issues/7224 https://www.malacards.org/card/plasminogen_deficiency_type_i Orphanet:722 MedDRA:10071570 hypoplasminogenemia ligneous conjunctivitis MESH:C580017 A rare multi-system disease characterized by markedly impaired extracellular fibrinolysis leading to the formation of ligneous (fibrin-rich) pseudomembranes on mucosae. type 1 plasminogen deficiency GARD:0004380 plasminogen deficiency type 1 icd11.foundation:1240776230 SCTID:95840007 plasminogen deficiency, type 1 MONDO:0009009 DOID:0111592 UMLS:C1968804 OMIM:217090 plasminogen deficiency, type I SCTID:403435005 Orphanet:97231 ICD9:372.39 MEDGEN:369859 inherited blood coagulation disorder chronic