Search Ontology:
Human Disease
plasminogen deficiency type I
- Term ID
- DOID:0111592
- Synonyms
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- hypoplasminogenemia
- 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. (4)
- References
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- GARD:4380
- ICD10CM:E88.02
- MESH:C566897
- MESH:C580017
- MIM:217090
- ORDO:722
- SNOMEDCT_US_2023_03_01:95840007
- SNOMEDCT_US_2023_03_01:95844003
- UMLS_CUI:C0398621
- UMLS_CUI:C1968804
- Ontology
- Human Disease ( DOID:0111592 )
- is a type of
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Genes Involved
Zebrafish Models