Major Hematological and Immunological Diagnoses Except Sickle Cell Crisis and Coagulation Disorders with CC

Principal diagnosis codes (63)

• D59.0Drug-induced autoimmune hemolytic anemia
• D59.10Autoimmune hemolytic anemia, unspecified
• D59.11Warm autoimmune hemolytic anemia
• D59.12Cold autoimmune hemolytic anemia
• D59.13Mixed type autoimmune hemolytic anemia
• D59.19Other autoimmune hemolytic anemia
• D59.2Drug-induced nonautoimmune hemolytic anemia
• D59.4Other nonautoimmune hemolytic anemias
• D59.5Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
• D59.6Hemoglobinuria due to hemolysis from other external causes
• D59.8Other acquired hemolytic anemias
• D59.9Acquired hemolytic anemia, unspecified
• D60.0Chronic acquired pure red cell aplasia
• D60.1Transient acquired pure red cell aplasia
• D60.8Other acquired pure red cell aplasias
• D60.9Acquired pure red cell aplasia, unspecified
• D61.01Constitutional (pure) red blood cell aplasia
• D61.02Shwachman-Diamond syndrome
• D61.03Fanconi anemia
• D61.09Other constitutional aplastic anemia
• D61.1Drug-induced aplastic anemia
• D61.2Aplastic anemia due to other external agents
• D61.3Idiopathic aplastic anemia
• D61.810Antineoplastic chemotherapy induced pancytopenia
• D61.811Other drug-induced pancytopenia
• D61.818Other pancytopenia
• D61.89Other specified aplastic anemias and other bone marrow failure syndromes
• D61.9Aplastic anemia, unspecified
• D70.0Congenital agranulocytosis
• D70.1Agranulocytosis secondary to cancer chemotherapy
• D70.2Other drug-induced agranulocytosis
• D70.3Neutropenia due to infection
• D70.4Cyclic neutropenia
• D70.8Other neutropenia
• D70.9Neutropenia, unspecified
• D71.1Leukocyte adhesion deficiency
• D71.8Other functional disorders of polymorphonuclear neutrophils
• D71.9Functional disorders of polymorphonuclear neutrophils, unspecified
• D72.0Genetic anomalies of leukocytes
• D80.6Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
• D80.8Other immunodeficiencies with predominantly antibody defects
• D80.9Immunodeficiency with predominantly antibody defects, unspecified
• D81.0Severe combined immunodeficiency [SCID] with reticular dysgenesis
• D81.1Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
• D81.2Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
• D81.4Nezelof's syndrome
• D81.6Major histocompatibility complex class I deficiency
• D81.7Major histocompatibility complex class II deficiency
• D81.82Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
• D81.89Other combined immunodeficiencies
• D81.9Combined immunodeficiency, unspecified
• D82.0Wiskott-Aldrich syndrome
• D82.1Di George's syndrome
• D89.810Acute graft-versus-host disease
• D89.811Chronic graft-versus-host disease
• D89.812Acute on chronic graft-versus-host disease
• D89.813Graft-versus-host disease, unspecified
• I27.841Fontan-associated lymphatic dysfunction
• T86.00Unspecified complication of bone marrow transplant
• T86.01Bone marrow transplant rejection
• T86.02Bone marrow transplant failure
• T86.03Bone marrow transplant infection
• T86.09Other complications of bone marrow transplant