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hypoplasminogenemia

Go to external page http://purl.obolibrary.org/obo/MONDO_0009009

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

Synonyms: hypoplasminogenemia plasminogen deficiency, type 1 type 1 plasminogen deficiency plasminogen deficiency type 1 plasminogen deficiency, type I

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:C580017 (MONDO:equivalentTo)
  • DOID:0111592 (MONDO:equivalentTo)
  • OMIM:217090 (Orphanet:722/e)
  • UMLS:C0398621 (Orphanet:722/e)
  • Orphanet:722 (OMIM:217090)
  • SCTID:95840007 (MONDO:equivalentTo)
  • GARD:4380 (Orphanet:722)
  • UMLS:C1274789 (OMIM:217090)
  • Orphanet:97231 (OMIM:217090)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/7100

exactMatch

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

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

http://purl.obolibrary.org/obo/DOID_0111592

https://omim.org/entry/217090

http://identifiers.org/mesh/C580017

http://identifiers.org/snomedct/95840007

has related synonym

ligneous conjunctivitis

id

MONDO:0009009

relatedMatch

http://www.orpha.net/ORDO/Orphanet_97231

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0009009