D82.0

Applicable To

• Immunodeficiency with thrombocytopenia and eczema

Approximate Synonyms

• Wiskott aldrich syndrome

Clinical Information

• A rare, x-linked immunodeficiency syndrome characterized by eczema, thrombocytopenia, and recurrent pyogenic infection. It is seen exclusively in young boys. Typically, igm levels are low and iga and ige levels are elevated. Lymphoreticular malignancies are common.

• A rare, x-linked immunodeficiency syndrome characterized by eczema; lymphopenia; and, recurrent pyogenic infection. It is seen exclusively in young boys. Typically, immunoglobulin m levels are low and immunoglobulin a and immunoglobulin e levels are elevated. Lymphoreticular malignancies are common.

• An inherited immune disorder that occurs in young boys. It causes eczema a type of skin inflammation), a decrease in the number of platelets blood cells that help prevent bleeding), and frequent bacterial infections. People with wiskott-aldrich syndrome are at increased risk of developing leukemia and lymphoma.

• Rare x-linked immunodeficiency syndrome of young boys characterized by eczema, thrombocytopenic purpura and recurrent pyogenic infection; igm levels are low and iga and ige levels are elevated; lymphoreticular malignancies are common.

Details

• D82.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• The 2023 edition of ICD-10-CM D82.0 became effective on October 1, 2022.

• This is the American ICD-10-CM version of D82.0 – other international versions of ICD-10 D82.0 may differ.