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Disease Ontology Browser
plasminogen deficiency type I (DOID:0111592)
Alliance: disease page
Synonyms: hypoplasminogenemia
Alt IDs: OMIM:217090, ICD10CM:E88.02, MESH:C566897, MESH:C580017, ORDO:722, UMLS_CUI:C0398621, UMLS_CUI:C1968804
Definition: 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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
05/19/2020
MGI 6.15
The Jackson Laboratory