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bn:03303533n
Noun Named Entity
SYL
No term available
EN
Haemophilia C is a mild form of haemophilia affecting both sexes, due to factor XI deficiency. Wikipedia
Relations
Sources
IS A
EN
rare disease
EN
hemophilia
EN
coagulopathy
GENETIC ASSOCIATION
EN
plasma thromboplastin antecedent
HEALTH SPECIALTY
EN
hematology
MODE OF INHERITANCE
EN
dominance
SYMPTOMS
EN
bleeding

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