|OBO ID: DOID:12259|
|Term Name:||hemophilia B||Search Ontology:|
|Definition:||A blood coagulation disease that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait. http://www.nlm.nih.gov/medlineplus/ency/article/000539.htm|
|Ontology:||Human Disease (DOID:12259)|
|is a type of:||
OTHER hemophilia B PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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