F8 C1,C2 domains variants [extracellular region]

Stable Identifier
R-HSA-9665818
Type
Complex
Species
Homo sapiens
Compartment
extracellular region
Synonyms
factor VIII variants with mutations in the C1, C2 domains
Locations in the PathwayBrowser
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Participants
components
Participates
as an input of
Disease
Name Identifier Synonyms
factor VIII deficiency DOID:12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
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