Term Name: plasminogen deficiency type I
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.
Ontology: Human Disease [DOID:0111592]   ( DOID:0111592 )

Relationships
is a type of: autosomal recessive disease syndrome