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DO Term : plasminogen deficiency type I [DOID:0111592] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndrome characterized by decreased serum plasminogen activity, decreased plasminogen antigen levels, and chronic mucosal pseudomembranous lesions typically manifesting as ligneous conjunctivitis that has_material_basis_in homozygous or compound heterozygous mutation in PLG on chromosome 6q26.
  • synonyms:
  • ICD10CM:E88.02,
  • UMLS_CUI:C1968804,
  • MESH:C580017,
  • GARD:4380,
  • MESH:C566897,
  • SNOMEDCT_US_2023_03_01:95840007,
  • ORDO:722,
  • 217090,
  • OMIM:217090,
  • SNOMEDCT_US_2023_03_01:95844003,
  • hypoplasminogenemia,
  • UMLS_CUI:C0398621
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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents