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Defective factor XII causes hereditary angioedema
An instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-9657688)
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Statements
instance of
biological pathway
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-9657688
part of
Defects of contact activation system (CAS) and kallikrein/kinin system (KKS)
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-9657688
found in taxon
Homo sapiens
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-9657688
exact match
https://identifiers.org/reactome:R-HSA-9657688
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-9657688
has part(s)
Cleavage of factor XII variant by activated thrombin
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-9657688
Cleavage of FXII variant by KLKB1
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-9657688
cites work
A mechanism for hereditary angioedema with normal C1 inhibitor: an inhibitory regulatory role for the factor XII heavy chain
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-9657688
Identifiers
Reactome ID
R-HSA-9657688
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-9657688
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