Z83.2

Applicable To

• Conditions classifiable to

Approximate Synonyms

• Family history of alpha thalassemia

• Family history of alpha thalassemia inherited anemia)

• Family history of anemia

• Family history of antithrombin 3 deficiency

• Family history of antithrombin 3 deficiency blood clots too easily)

• Family history of beta thalassemia

• Family history of beta thalassemia inherited anemia)

• Family history of bleeding disorder

• Family history of blood disorder

• 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 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 sickle cell anemia

• Family history of von willebrand disease

• Family history of von willebrand disease blood clots too slowly)

• Fh: anemia

• Fh: blood disorder

• Fh: sickle cell anemia

Present On Admission

• Z83.2

Details

• Z83.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• Short description: Family history of dis of the bld/bld-form org/immun mechnsm

• The 2023 edition of ICD-10-CM Z83.2 became effective on October 1, 2022.

• This is the American ICD-10-CM version of Z83.2 – other international versions of ICD-10 Z83.2 may differ.