Search Ontology:
Human Disease

plasminogen deficiency type I

Term ID
DOID:0111592
Synonyms
  • 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
Ontology
Human Disease   ( DOID:0111592 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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