ICD-10-CM/PCS MS-DRG v40.1 Definitions Manual

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MDC 16 Diseases and disorders of blood, blood forming organs and immunologic disorders
Assignment of Diagnosis Codes
A182Tuberculous peripheral lymphadenopathy
A1885Tuberculosis of spleen
A281Cat-scratch disease
D150Benign neoplasm of thymus
D181Lymphangioma, any site
D360Benign neoplasm of lymph nodes
D3A091Benign carcinoid tumor of the thymus
D460Refractory anemia without ring sideroblasts, so stated
D461Refractory anemia with ring sideroblasts
D4620Refractory anemia with excess of blasts, unspecified
D4621Refractory anemia with excess of blasts 1
D4622Refractory anemia with excess of blasts 2
D464Refractory anemia, unspecified
D469Myelodysplastic syndrome, unspecified
D46ARefractory cytopenia with multilineage dysplasia
D46BRefractory cytopenia with multilineage dysplasia and ring sideroblasts
D46CMyelodysplastic syndrome with isolated del(5q) chromosomal abnormality
D46ZOther myelodysplastic syndromes
D472Monoclonal gammopathy
D473Essential (hemorrhagic) thrombocythemia
D500Iron deficiency anemia secondary to blood loss (chronic)
D501Sideropenic dysphagia
D508Other iron deficiency anemias
D509Iron deficiency anemia, unspecified
D510Vitamin B12 deficiency anemia due to intrinsic factor deficiency
D511Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
D512Transcobalamin II deficiency
D513Other dietary vitamin B12 deficiency anemia
D518Other vitamin B12 deficiency anemias
D519Vitamin B12 deficiency anemia, unspecified
D520Dietary folate deficiency anemia
D521Drug-induced folate deficiency anemia
D528Other folate deficiency anemias
D529Folate deficiency anemia, unspecified
D530Protein deficiency anemia
D531Other megaloblastic anemias, not elsewhere classified
D532Scorbutic anemia
D538Other specified nutritional anemias
D539Nutritional anemia, unspecified
D550Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
D551Anemia due to other disorders of glutathione metabolism
D5521Anemia due to pyruvate kinase deficiency
D5529Anemia due to other disorders of glycolytic enzymes
D553Anemia due to disorders of nucleotide metabolism
D558Other anemias due to enzyme disorders
D559Anemia due to enzyme disorder, unspecified
D560Alpha thalassemia
D561Beta thalassemia
D562Delta-beta thalassemia
D563Thalassemia minor
D564Hereditary persistence of fetal hemoglobin [HPFH]
D565Hemoglobin E-beta thalassemia
D568Other thalassemias
D569Thalassemia, unspecified
D5700Hb-SS disease with crisis, unspecified
D5701Hb-SS disease with acute chest syndrome
D5702Hb-SS disease with splenic sequestration
D5703Hb-SS disease with cerebral vascular involvement
D5709Hb-SS disease with crisis with other specified complication
D571Sickle-cell disease without crisis
D5720Sickle-cell/Hb-C disease without crisis
D57211Sickle-cell/Hb-C disease with acute chest syndrome
D57212Sickle-cell/Hb-C disease with splenic sequestration
D57213Sickle-cell/Hb-C disease with cerebral vascular involvement
D57218Sickle-cell/Hb-C disease with crisis with other specified complication
D57219Sickle-cell/Hb-C disease with crisis, unspecified
D573Sickle-cell trait
D5740Sickle-cell thalassemia without crisis
D57411Sickle-cell thalassemia, unspecified, with acute chest syndrome
D57412Sickle-cell thalassemia, unspecified, with splenic sequestration
D57413Sickle-cell thalassemia, unspecified, with cerebral vascular involvement
D57418Sickle-cell thalassemia, unspecified, with crisis with other specified complication
D57419Sickle-cell thalassemia, unspecified, with crisis
D5742Sickle-cell thalassemia beta zero without crisis
D57431Sickle-cell thalassemia beta zero with acute chest syndrome
D57432Sickle-cell thalassemia beta zero with splenic sequestration
D57433Sickle-cell thalassemia beta zero with cerebral vascular involvement
D57438Sickle-cell thalassemia beta zero with crisis with other specified complication
D57439Sickle-cell thalassemia beta zero with crisis, unspecified
D5744Sickle-cell thalassemia beta plus without crisis
D57451Sickle-cell thalassemia beta plus with acute chest syndrome
D57452Sickle-cell thalassemia beta plus with splenic sequestration
D57453Sickle-cell thalassemia beta plus with cerebral vascular involvement
D57458Sickle-cell thalassemia beta plus with crisis with other specified complication
D57459Sickle-cell thalassemia beta plus with crisis, unspecified
D5780Other sickle-cell disorders without crisis
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57813Other sickle-cell disorders with cerebral vascular involvement
D57818Other sickle-cell disorders with crisis with other specified complication
D57819Other sickle-cell disorders with crisis, unspecified
D580Hereditary spherocytosis
D581Hereditary elliptocytosis
D582Other hemoglobinopathies
D588Other specified hereditary hemolytic anemias
D589Hereditary hemolytic anemia, unspecified
D590Drug-induced autoimmune hemolytic anemia
D5910Autoimmune hemolytic anemia, unspecified
D5911Warm autoimmune hemolytic anemia
D5912Cold autoimmune hemolytic anemia
D5913Mixed type autoimmune hemolytic anemia
D5919Other autoimmune hemolytic anemia
D592Drug-induced nonautoimmune hemolytic anemia
D5930Hemolytic-uremic syndrome, unspecified
D5931Infection-associated hemolytic-uremic syndrome
D5932Hereditary hemolytic-uremic syndrome
D5939Other hemolytic-uremic syndrome
D594Other nonautoimmune hemolytic anemias
D595Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
D596Hemoglobinuria due to hemolysis from other external causes
D598Other acquired hemolytic anemias
D599Acquired hemolytic anemia, unspecified
D600Chronic acquired pure red cell aplasia
D601Transient acquired pure red cell aplasia
D608Other acquired pure red cell aplasias
D609Acquired pure red cell aplasia, unspecified
D6101Constitutional (pure) red blood cell aplasia
D6109Other constitutional aplastic anemia
D611Drug-induced aplastic anemia
D612Aplastic anemia due to other external agents
D613Idiopathic aplastic anemia
D61810Antineoplastic chemotherapy induced pancytopenia
D61811Other drug-induced pancytopenia
D61818Other pancytopenia
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D62Acute posthemorrhagic anemia
D630Anemia in neoplastic disease
D631Anemia in chronic kidney disease
D638Anemia in other chronic diseases classified elsewhere
D640Hereditary sideroblastic anemia
D641Secondary sideroblastic anemia due to disease
D642Secondary sideroblastic anemia due to drugs and toxins
D643Other sideroblastic anemias
D644Congenital dyserythropoietic anemia
D6481Anemia due to antineoplastic chemotherapy
D6489Other specified anemias
D649Anemia, unspecified
D65Disseminated intravascular coagulation [defibrination syndrome]
D66Hereditary factor VIII deficiency
D67Hereditary factor IX deficiency
D6800Von Willebrand disease, unspecified
D6801Von Willebrand disease, type 1
D68020Von Willebrand disease, type 2A
D68021Von Willebrand disease, type 2B
D68022Von Willebrand disease, type 2M
D68023Von Willebrand disease, type 2N
D68029Von Willebrand disease, type 2, unspecified
D6803Von Willebrand disease, type 3
D6804Acquired von Willebrand disease
D6809Other von Willebrand disease
D681Hereditary factor XI deficiency
D682Hereditary deficiency of other clotting factors
D68311Acquired hemophilia
D68312Antiphospholipid antibody with hemorrhagic disorder
D68318Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D6832Hemorrhagic disorder due to extrinsic circulating anticoagulants
D684Acquired coagulation factor deficiency
D6851Activated protein C resistance
D6852Prothrombin gene mutation
D6859Other primary thrombophilia
D6861Antiphospholipid syndrome
D6862Lupus anticoagulant syndrome
D6869Other thrombophilia
D688Other specified coagulation defects
D689Coagulation defect, unspecified
D690Allergic purpura
D691Qualitative platelet defects
D692Other nonthrombocytopenic purpura
D693Immune thrombocytopenic purpura
D6941Evans syndrome
D6942Congenital and hereditary thrombocytopenia purpura
D6949Other primary thrombocytopenia
D6951Posttransfusion purpura
D6959Other secondary thrombocytopenia
D696Thrombocytopenia, unspecified
D698Other specified hemorrhagic conditions
D699Hemorrhagic condition, unspecified
D700Congenital agranulocytosis
D701Agranulocytosis secondary to cancer chemotherapy
D702Other drug-induced agranulocytosis
D703Neutropenia due to infection
D704Cyclic neutropenia
D708Other neutropenia
D709Neutropenia, unspecified
D71Functional disorders of polymorphonuclear neutrophils
D720Genetic anomalies of leukocytes
D7210Eosinophilia, unspecified
D72110Idiopathic hypereosinophilic syndrome [IHES]
D72111Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
D72118Other hypereosinophilic syndrome
D72119Hypereosinophilic syndrome [HES], unspecified
D7212Drug rash with eosinophilia and systemic symptoms syndrome
D7218Eosinophilia in diseases classified elsewhere
D7219Other eosinophilia
D72818Other decreased white blood cell count
D72819Decreased white blood cell count, unspecified
D72820Lymphocytosis (symptomatic)
D72821Monocytosis (symptomatic)
D72823Leukemoid reaction
D72828Other elevated white blood cell count
D72829Elevated white blood cell count, unspecified
D7289Other specified disorders of white blood cells
D729Disorder of white blood cells, unspecified
D732Chronic congestive splenomegaly
D733Abscess of spleen
D734Cyst of spleen
D735Infarction of spleen
D7381Neutropenic splenomegaly
D7389Other diseases of spleen
D739Disease of spleen, unspecified
D740Congenital methemoglobinemia
D748Other methemoglobinemias
D749Methemoglobinemia, unspecified
D750Familial erythrocytosis
D751Secondary polycythemia
D75821Non-immune heparin-induced thrombocytopenia
D75822Immune-mediated heparin-induced thrombocytopenia
D75828Other heparin-induced thrombocytopenia syndrome
D75829Heparin-induced thrombocytopenia, unspecified
D75838Other thrombocytosis
D75839Thrombocytosis, unspecified
D7584Other platelet-activating anti-PF4 disorders
D7589Other specified diseases of blood and blood-forming organs
D759Disease of blood and blood-forming organs, unspecified
D75AGlucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
D761Hemophagocytic lymphohistiocytosis
D762Hemophagocytic syndrome, infection-associated
D763Other histiocytosis syndromes
D77Other disorders of blood and blood-forming organs in diseases classified elsewhere
D800Hereditary hypogammaglobulinemia
D801Nonfamilial hypogammaglobulinemia
D802Selective deficiency of immunoglobulin A [IgA]
D803Selective deficiency of immunoglobulin G [IgG] subclasses
D804Selective deficiency of immunoglobulin M [IgM]
D805Immunodeficiency with increased immunoglobulin M [IgM]
D806Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D807Transient hypogammaglobulinemia of infancy
D808Other immunodeficiencies with predominantly antibody defects
D809Immunodeficiency with predominantly antibody defects, unspecified
D810Severe combined immunodeficiency [SCID] with reticular dysgenesis
D811Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
D812Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
D814Nezelof's syndrome
D816Major histocompatibility complex class I deficiency
D817Major histocompatibility complex class II deficiency
D8182Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
D8189Other combined immunodeficiencies
D819Combined immunodeficiency, unspecified
D820Wiskott-Aldrich syndrome
D821Di George's syndrome
D822Immunodeficiency with short-limbed stature
D823Immunodeficiency following hereditary defective response to Epstein-Barr virus
D824Hyperimmunoglobulin E [IgE] syndrome
D828Immunodeficiency associated with other specified major defects
D829Immunodeficiency associated with major defect, unspecified
D830Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D831Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
D832Common variable immunodeficiency with autoantibodies to B- or T-cells
D838Other common variable immunodeficiencies
D839Common variable immunodeficiency, unspecified
D840Lymphocyte function antigen-1 [LFA-1] defect
D8481Immunodeficiency due to conditions classified elsewhere
D84821Immunodeficiency due to drugs
D84822Immunodeficiency due to external causes
D8489Other immunodeficiencies
D849Immunodeficiency, unspecified
D890Polyclonal hypergammaglobulinemia
D892Hypergammaglobulinemia, unspecified
D893Immune reconstitution syndrome
D8940Mast cell activation, unspecified
D8941Monoclonal mast cell activation syndrome
D8942Idiopathic mast cell activation syndrome
D8943Secondary mast cell activation
D8944Hereditary alpha tryptasemia
D8949Other mast cell activation disorder
D89810Acute graft-versus-host disease
D89811Chronic graft-versus-host disease
D89812Acute on chronic graft-versus-host disease
D89813Graft-versus-host disease, unspecified
D89831Cytokine release syndrome, grade 1
D89832Cytokine release syndrome, grade 2
D89833Cytokine release syndrome, grade 3
D89834Cytokine release syndrome, grade 4
D89835Cytokine release syndrome, grade 5
D89839Cytokine release syndrome, grade unspecified
D8989Other specified disorders involving the immune mechanism, not elsewhere classified
D899Disorder involving the immune mechanism, unspecified
E320Persistent hyperplasia of thymus
E321Abscess of thymus
E328Other diseases of thymus
E329Disease of thymus, unspecified
I881Chronic lymphadenitis, except mesenteric
I888Other nonspecific lymphadenitis
I889Nonspecific lymphadenitis, unspecified
I898Other specified noninfective disorders of lymphatic vessels and lymph nodes
I899Noninfective disorder of lymphatic vessels and lymph nodes, unspecified
L040Acute lymphadenitis of face, head and neck
L041Acute lymphadenitis of trunk
L042Acute lymphadenitis of upper limb
L043Acute lymphadenitis of lower limb
L048Acute lymphadenitis of other sites
L049Acute lymphadenitis, unspecified
Q8901Asplenia (congenital)
Q8909Congenital malformations of spleen
R161Splenomegaly, not elsewhere classified
R233Spontaneous ecchymoses
R590Localized enlarged lymph nodes
R591Generalized enlarged lymph nodes
R599Enlarged lymph nodes, unspecified
R710Precipitous drop in hematocrit
R718Other abnormality of red blood cells
R75Inconclusive laboratory evidence of human immunodeficiency virus [HIV]
R760Raised antibody titer
R768Other specified abnormal immunological findings in serum
R769Abnormal immunological finding in serum, unspecified
S3600XAUnspecified injury of spleen, initial encounter
S36020AMinor contusion of spleen, initial encounter
S36021AMajor contusion of spleen, initial encounter
S36029AUnspecified contusion of spleen, initial encounter
S36030ASuperficial (capsular) laceration of spleen, initial encounter
S36031AModerate laceration of spleen, initial encounter
S36032AMajor laceration of spleen, initial encounter
S36039AUnspecified laceration of spleen, initial encounter
S3609XAOther injury of spleen, initial encounter
T8030XAABO incompatibility reaction due to transfusion of blood or blood products, unspecified, initial encounter
T80310AABO incompatibility with acute hemolytic transfusion reaction, initial encounter
T80311AABO incompatibility with delayed hemolytic transfusion reaction, initial encounter
T80319AABO incompatibility with hemolytic transfusion reaction, unspecified, initial encounter
T8039XAOther ABO incompatibility reaction due to transfusion of blood or blood products, initial encounter
T8040XARh incompatibility reaction due to transfusion of blood or blood products, unspecified, initial encounter
T80410ARh incompatibility with acute hemolytic transfusion reaction, initial encounter
T80411ARh incompatibility with delayed hemolytic transfusion reaction, initial encounter
T80419ARh incompatibility with hemolytic transfusion reaction, unspecified, initial encounter
T8049XAOther Rh incompatibility reaction due to transfusion of blood or blood products, initial encounter
T8082XAComplication of immune effector cellular therapy, initial encounter
T8089XAOther complications following infusion, transfusion and therapeutic injection, initial encounter
T80910AAcute hemolytic transfusion reaction, unspecified incompatibility, initial encounter
T80911ADelayed hemolytic transfusion reaction, unspecified incompatibility, initial encounter
T80919AHemolytic transfusion reaction, unspecified incompatibility, unspecified as acute or delayed, initial encounter
T8092XAUnspecified transfusion reaction, initial encounter
T80A0XANon-ABO incompatibility reaction due to transfusion of blood or blood products, unspecified, initial encounter
T80A10ANon-ABO incompatibility with acute hemolytic transfusion reaction, initial encounter
T80A11ANon-ABO incompatibility with delayed hemolytic transfusion reaction, initial encounter
T80A19ANon-ABO incompatibility with hemolytic transfusion reaction, unspecified, initial encounter
T80A9XAOther non-ABO incompatibility reaction due to transfusion of blood or blood products, initial encounter
T8600Unspecified complication of bone marrow transplant
T8601Bone marrow transplant rejection
T8602Bone marrow transplant failure
T8603Bone marrow transplant infection
T8609Other complications of bone marrow transplant
Z9481Bone marrow transplant status
Z9484Stem cells transplant status

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18 Jan 2023 08:46:59
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