Severe hypoplasminogenemia (HPG) or type 1 plasminogen (plg) deficiency is a systemic disease characterised by markedly impaired extracellular fibrinolysis leading to the formation of ligneous (fibrin-rich) pseudomembranes on mucosae during wound healing. [ Orphanet:722 ]

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0398621 (Orphanet:722)
  • UMLS:C1968804 (Orphanet:722)
  • ICD10:L90.5 (Orphanet:722)
  • MESH:C580017 (MONDO:equivalentTo)
  • GARD:0004380 (Orphanet-shared)
  • OMIM:217090 (Orphanet:722)
  • SCTID:95840007 (MONDO:equivalentTo)
  • Orphanet:722 (OMIM:217090)
Subsets

ordo_disease

definition

Severe hypoplasminogenemia (HPG) or type 1 plasminogen (plg) deficiency is a systemic disease characterised by markedly impaired extracellular fibrinolysis leading to the formation of ligneous (fibrin-rich) pseudomembranes on mucosae during wound healing.

exactMatch

http://linkedlifedata.com/resource/umls/id/C0398621

http://www.orpha.net/ORDO/Orphanet_722

http://identifiers.org/omim/217090

http://linkedlifedata.com/resource/umls/id/C1968804

http://identifiers.org/mesh/C580017

http://identifiers.org/snomedct/95840007

has exact synonym

plasminogen deficiency type 1

has related synonym

plasminogen deficiency, type 2

Dysplasminogenemia

plasminogen deficiency, type 1

type 1 plasminogen deficiency

ligneous conjunctivitis

plasminogen deficiency, type I

id

MONDO:0009009