Specific code 2010 ICD-9-CM Diagnosis Code V18.3
Family history of other blood disorders
  • Short description: Fam hx-blood disord NEC.
  • ICD-9-CM V18.3 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM V18.3 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
  • You are viewing the 2010 version of ICD-9-CM V18.3.
  • More recent version(s) of ICD-9-CM V18.3: 2011 2012 2013 2014.
Disease Synonyms
  • Family history of antithrombin 3 deficiency
  • Family history of antithrombin 3 deficiency (blood clots too easily)
  • Family history of bleeding disorder
  • Family history of blood disorder
  • Family history of familial hypercholesterolemia
  • Family history of hemoglobinopathy
  • Family history of hemoglobinopathy (abnormal hemoglobin)
  • Family history of hemoglobinopathy C
  • Family history of hemoglobinopathy C (abnormal hemoglobin)
  • Family history of hemoglobinopathy E
  • Family history of hemoglobinopathy E (abnormal hemoglobin)
  • Family history of hemophilia
  • Family history of hypercoagulable state
  • Family history of hypercoagulable state (blood clots too easily)
  • Family history of impaired glucose tolerance
  • Family history of protein C deficiency
  • Family history of protein C deficiency (blood clots too easily)
  • Family history of protein C resistance
  • Family history of protein C resistance (blood clots too easily)
  • Family history of protein S deficiency
  • Family history of protein S deficiency (blood clots too easily)
  • Family history of pseudocholinesterase deficiency
  • Family history of pseudocholinesterase deficiency (inherited enzyme disorder)
  • Family history of Von Willebrand disease
  • Family history of von Willebrand disease (blood clots too slowly)
  • Family history: Blood disorder
  • Family history: Hemophilia
  • Family history: Sickle cell trait
  • Family history: Spherocytosis
  • FH: Blood disorder
  • Fhx of antithrombin 3 deficiency
  • Fhx of bleeding disorder
  • Fhx of blood disorder
  • Fhx of hemoglobinopathy
  • Fhx of hemoglobinopathy C
  • Fhx of hemoglobinopathy E
  • Fhx of hemophilia
  • Fhx of hypercoagulable state
  • Fhx of protein C deficiency
  • Fhx of protein C resistance
  • Fhx of protein S deficiency
  • Fhx of pseudocholinesterase deficiency
  • Fhx of von Willebrand disease
  • Spouse hemophiliac
Convert to ICD-10-CM: V18.3 converts approximately to:
  • 2014 ICD-10-CM Z83.2 Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
ICD-9-CM Volume 2 Index entries containing back-references to V18.3:
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM V18.3 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2010 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.