ICD-9-CM 279.41 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 279.41 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
An autoimmune hematologic disorder characterized by autoimmune hemolytic anemia, thrombocytopenia, lymphadenopathy, hepatomegaly and splenomegaly. Patients are at an increased risk of developing hodgkin and non-hodgkin lymphomas
Rare congenital lymphoid disorder due to mutations in certain fas-fas ligand pathway genes. Known causes include mutations in fas, tnfsf6, nras, casp8, and casp10 proteins. Clinical features include lymphadenopathy; splenomegaly; and autoimmunity