2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 > Coagulation Defects 286.* >
 2007 ICD-9-CM Diagnosis 286.7
Acquired coagulation factor deficiency On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date.
The 2009 version of ICD-9-CM 286.7 can be accessed here. - 286.7 is a specific code that can be used to specify a diagnosis
- 286.7 contains 17 index entries
- View the ICD-9-CM Volume 1 286.* hierarchy
286.7 also known as:- Deficiency of coagulation factor due to:
- liver disease
- vitamin K deficiency
- Hypoprothrombinemia, acquired
Use additional E-code to identify cause, if drug-induced 286.7 excludes: - vitamin K deficiency of newborn (776.0)
Index entries containing 286.7:- Defect, defective 759.9
- coagulation (factor) (see also Deficiency, coagulation factor) 286.9
- acquired (any)
 286.7
- due to
- liver disease 286.7
- vitamin K deficiency 286.7
Deficiency, deficient- AC globulin (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
- coagulation factor NEC 286.9
- acquired (any) 286.7
- due to
- liver disease 286.7
- vitamin K deficiency 286.7
- factor (see also Defect, coagulation) 286.9
- multiple (congenital) 286.9
- acquired 286.7
- fibrin-stabilizing factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
- labile factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
- proaccelerin (congenital) (see also Defect, congenital) 286.3
- acquired 286.7
- proconvertin factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
- prothrombin (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
- stable factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
Hemophilia (familial) (hereditary) 286.0- calcipriva (see also Fibrinolysis) 286.7
- nonfamilial 286.7
Hypoprothrombinemia (congenital) (hereditary) (idiopathic) (see also Defect, coagulation) 286.3- acquired 286.7
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