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Factor Vii Deficiency

Disease ID: disease_node_3140

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DbxrefGARD:2238, ICD10CM:D68.2, MESH:D005168, MIM:227500, NCI:C131631, ORDO:327, SNOMEDCT_US_2023_03_01:154820003, UMLS_CUI:C0015503
SubclassofDOID_0050737, DOID_1247
Data SourceDOID, MESH
Synonymsdeficiency, stable
Mesh IdD005168
Mesh LabelFactor VII Deficiency
Disease Has FeatureDOID_801
Mesh SubclassofD020147, D025861, D006474
Doid Labelfactor VII deficiency
Doid DescriptionA 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.
Has SymptomSYMP_0000756, SYMP_0000742, SYMP_0000007, SYMP_0000448
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_3140
Doid IdDOID_2215
LabelFactor Vii Deficiency