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286.0 CONG FACTOR VIII DIORD


Code Information

Diagnosis Code: 286.0

Short Description: Cong factor viii diord

Long Description: Congenital factor VIII disorder

Code Classification:

  • Diseases of the blood and blood-forming organs (280–289)
    • Diseases of the blood and blood-forming organs (280-289)
      • 286 Coagulation defects
        • 286.0 Cong factor viii diord

Code Version: 2015 ICD-9-CM


References to Index of Diseases and Injuries

The code 286.0 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Arthritis, arthritic (acute) (chronic) (subacute) 716.9
    • due to or associated with
      • hemophilia (see also Hemophilia) 286.0 [713.2]
  • Deficiency, deficient
    • antihemophilic
      • factor (A) 286.0
        • B 286.1
        • C 286.2
      • globulin (AHG) NEC 286.0
    • factor (see also Defect, coagulation) 286.9
      • VIII (congenital) (functional) 286.0
        • with
          • functional defect 286.0
          • vascular defect 286.4
  • Disease, diseased - see also Syndrome
    • bleeder's 286.0
  • Disorder - see also Disease
    • coagulation (factor) (see also Defect, coagulation) 286.9
      • factor VIII (congenital) (functional) 286.0
    • factor, coagulation (see also Defect, coagulation) 286.9
      • VIII (congenital) (functional) 286.0
  • Hemophilia (familial) (hereditary) 286.0
    • A 286.0
      • carrier (asymptomatic) V83.01
        • symptomatic V83.02
    • acquired 286.52
    • autoimmune 286.52
    • B (Leyden) 286.1
    • C 286.2
    • calcipriva (see also Fibrinolysis) 286.7
    • classical 286.0
    • nonfamilial 286.7
    • secondary 286.52
    • vascular 286.4
  • Hemorrhage, hemorrhagic (nontraumatic) 459.0
    • pregnancy (concealed) 641.9
      • due to
        • afibrinogenemia or other coagulation defect (conditions classifiable to 286.0-286.9) 641.3
          • affecting fetus or newborn 762.1
  • Pregnancy (single) (uterine) (without sickness) V22.2
    • complicated (by) 646.9
      • hemorrhage 641.9
        • due to
          • afibrinogenemia or other coagulation defect (conditions classifiable to 286.0-286.9) 641.3
  • Subhemophilia 286.0

Crosswalk Information

The code 286.0 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
286.0 Right Arrow D66 Hereditary factor VIII deficiency
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
286.1 Congenital factor IX disorder
286.2 Congenital factor XI deficiency
286.3 Congenital deficiency of other clotting factors
286.4 Von Willebrand's disease
286.52 Acquired hemophilia
286.53 Antiphospholipid antibody with hemorrhagic disorder
286.59 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
286.6 Defibrination syndrome
286.7 Acquired coagulation factor deficiency
286.9 Other and unspecified coagulation defects

This page was last updated on: 10/1/2014

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