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Agent Commons
Collaborative Research
Diseases
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Hematologic disorder
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Blood coagulation disease
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Inherited blood coagulation disorder
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Inherited thrombophilia
Thrombophilia, X-linked, due to factor 8 defect
rare
Identifiers
MONDO:0859082
OMIM:301071
Causal genes
F8
Part of
Inherited thrombophilia
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