FVIII variant:vWF multimer [extracellular region]

Stable Identifier
R-HSA-9666393
Type
Complex
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Participates
Disease
Name Identifier Synonyms
factor VIII deficiency DOID:12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
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