|OBO ID: DOID:2215|
|Term Name:||factor VII deficiency||Search Ontology:|
|Definition:||A blood coagulation disease that is characterized by easy bleeding, has_symptom epistaxis, bleeding of the gums, menorrhagia, and occasionally hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation in the F7 gene, which encodes coagulation factor VII, an important factor in the clotting cascade. (2)|
|Ontology:||Human Disease (DOID:2215)|
|is a type of:||
OTHER factor VII deficiency PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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