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