Diseases of the Blood and Blood-Forming Organs 280-289 by International Classification of Diseases Lyrics
Diseases of the blood and blood-forming organs (280–289)Anemia (280–285)(280) Iron deficiency anemias
(280.0) Iron deficiency anemia secondary to blood loss (chronic)
(280.1) Iron deficiency anemia secondary to inadequate dietary iron intake
(280.8) Other specified iron deficiency anemias
(280.9) Iron deficiency anemia, unspecified
(281) Other deficiency anemias
(281.0) pernicious anemia
(281.2) Anemia, folate deficiency
(281.3) Other specified megaloblastic anemias, not elsewhere classified
(282) Hereditary hemolytic anemias
(282.0) Hereditary spherocytosis
(282.2) G6PD
(282.5) Sickle-cell trait
(282.6) Sickle-cell anemia
(283) Acquired hemolytic anemias
(283.0) Autoimmune hemolytic anemias
-Warm autoimmune hemolytic anemia
(283.1) Non-autoimmune hemolytic anemias
(283.2) Hemoglobinuria due to hemolysis from external causes
-Paroxysmal nocturnal hemoglobinuria
(284) Aplastic anemia
(284.0) Constitutional aplastic anemia
(284.01) Constitutional red blood cell aplasia
(284.09) Other constitutional aplastic anemia
(284.1) Pancytopenia
(284.2) Myelophthisis
(284.8) Other specified aplastic anemias
(284.81) Other specified aplastic anemias
(284.89) Red cell aplasia
(284.9) Aplastic anemia unspecified
(285) Other and unspecified anemias
(285.0) Sideroblastic anemia
(285.1) Acute posthemorrhagic anemia
(285.2) Anemia in chronic illness
(285.21) Anemia in chronic kidney disease
(285.22) Anemia in neoplastic disease
(285.29) Anemia of other chronic illness
(285.3) Antineoplastic chemotherapy induced anemia
(285.8) Other specified anemias
(285.9) Anemia unspecifiedCoagulation/hemorrhagic (286–287)(286) Coagulation defects
(286.0) Haemophilia A
(286.1) Haemophilia B
(286.2) Haemophilia C
(286.3) Congenital deficiency of other clotting factors
-Factor XIII deficiency
(286.4) Von Willebrand's disease
(286.5) Hemorrhagic disorder due to intrinsic anticoagulants
(286.6) Defibrination syndrome
(286.7) Acquired coagulation factor deficiency
(286.9) Coagulation defects, other
(287) Purpura and other hemorrhagic conditions
(287.0) Allergic purpura
-Henoch-Schönlein purpura
(287.3) Thrombocytopenia, primary
(287.31) Immune thrombocytopenic purpura
-Idiopathic thrombocytopenic purpura
(287.4) Thrombocytopenia, secondary
(287.9) Hemorrhagic conditions, unspec.Other (288–289)(288) Diseases of white blood cells
(288.0) Leukopenia
(288.1) Functional disorders of polymorphonuclear neutrophils
(288.2) Genetic anomalies of leukocytes
(288.3) Eosinophilia
(288.4) Hemophagocytic syndromes
(288.5) Decreased white blood cell count
(288.50) Leukocytopenia, unspecified
(288.51) Lymphocytopenia
(288.6) Elevated white blood cell count
(288.60) Leukocytosis, unspecified
(288.61) Lymphocytosis (symptomatic)
(288.62) Leukemoid reaction
(288.63) Monocytosis (symptomatic)
(288.64) Plasmacytosis
(288.65) Basophilia
(288.66) Bandemia
(288.8) Other specified disease of white blood cells
(288.9) Abnormal white blood cells, unspec.
(289) Other diseases of blood and blood-forming organs
(289.0) Polycythemia secondary
(289.1) Chronic lymphadenitis
(289.2) Nonspecific mesenteric lymphadenitis
(289.3) Lymphadenitis unspecified except mesenteric
(289.4) Hypersplenism
(289.5) Other diseases of spleen
(289.50) Disease of spleen unspecified
(289.51) Chronic congestive splenomegaly
(289.52) Splenic sequestration
(289.53) Neutropenic splenomegaly
(289.59) Other diseases of spleen
(289.6) Familial polycythemia
(289.7) Methemoglobinemia
(289.8) Other specified diseases of blood and blood-forming organs
(289.81) Primary hypercoagulable state
(289.82) Secondary hypercoagulable state
(289.83) Myelofibrosis
(289.84) Heparin-induced thrombocytopenia
(289.89) Other specified diseases of blood and blood-forming organs
(289.9) Unspecified diseases of blood and blood-forming organs
(280.0) Iron deficiency anemia secondary to blood loss (chronic)
(280.1) Iron deficiency anemia secondary to inadequate dietary iron intake
(280.8) Other specified iron deficiency anemias
(280.9) Iron deficiency anemia, unspecified
(281) Other deficiency anemias
(281.0) pernicious anemia
(281.2) Anemia, folate deficiency
(281.3) Other specified megaloblastic anemias, not elsewhere classified
(282) Hereditary hemolytic anemias
(282.0) Hereditary spherocytosis
(282.2) G6PD
(282.5) Sickle-cell trait
(282.6) Sickle-cell anemia
(283) Acquired hemolytic anemias
(283.0) Autoimmune hemolytic anemias
-Warm autoimmune hemolytic anemia
(283.1) Non-autoimmune hemolytic anemias
(283.2) Hemoglobinuria due to hemolysis from external causes
-Paroxysmal nocturnal hemoglobinuria
(284) Aplastic anemia
(284.0) Constitutional aplastic anemia
(284.01) Constitutional red blood cell aplasia
(284.09) Other constitutional aplastic anemia
(284.1) Pancytopenia
(284.2) Myelophthisis
(284.8) Other specified aplastic anemias
(284.81) Other specified aplastic anemias
(284.89) Red cell aplasia
(284.9) Aplastic anemia unspecified
(285) Other and unspecified anemias
(285.0) Sideroblastic anemia
(285.1) Acute posthemorrhagic anemia
(285.2) Anemia in chronic illness
(285.21) Anemia in chronic kidney disease
(285.22) Anemia in neoplastic disease
(285.29) Anemia of other chronic illness
(285.3) Antineoplastic chemotherapy induced anemia
(285.8) Other specified anemias
(285.9) Anemia unspecifiedCoagulation/hemorrhagic (286–287)(286) Coagulation defects
(286.0) Haemophilia A
(286.1) Haemophilia B
(286.2) Haemophilia C
(286.3) Congenital deficiency of other clotting factors
-Factor XIII deficiency
(286.4) Von Willebrand's disease
(286.5) Hemorrhagic disorder due to intrinsic anticoagulants
(286.6) Defibrination syndrome
(286.7) Acquired coagulation factor deficiency
(286.9) Coagulation defects, other
(287) Purpura and other hemorrhagic conditions
(287.0) Allergic purpura
-Henoch-Schönlein purpura
(287.3) Thrombocytopenia, primary
(287.31) Immune thrombocytopenic purpura
-Idiopathic thrombocytopenic purpura
(287.4) Thrombocytopenia, secondary
(287.9) Hemorrhagic conditions, unspec.Other (288–289)(288) Diseases of white blood cells
(288.0) Leukopenia
(288.1) Functional disorders of polymorphonuclear neutrophils
(288.2) Genetic anomalies of leukocytes
(288.3) Eosinophilia
(288.4) Hemophagocytic syndromes
(288.5) Decreased white blood cell count
(288.50) Leukocytopenia, unspecified
(288.51) Lymphocytopenia
(288.6) Elevated white blood cell count
(288.60) Leukocytosis, unspecified
(288.61) Lymphocytosis (symptomatic)
(288.62) Leukemoid reaction
(288.63) Monocytosis (symptomatic)
(288.64) Plasmacytosis
(288.65) Basophilia
(288.66) Bandemia
(288.8) Other specified disease of white blood cells
(288.9) Abnormal white blood cells, unspec.
(289) Other diseases of blood and blood-forming organs
(289.0) Polycythemia secondary
(289.1) Chronic lymphadenitis
(289.2) Nonspecific mesenteric lymphadenitis
(289.3) Lymphadenitis unspecified except mesenteric
(289.4) Hypersplenism
(289.5) Other diseases of spleen
(289.50) Disease of spleen unspecified
(289.51) Chronic congestive splenomegaly
(289.52) Splenic sequestration
(289.53) Neutropenic splenomegaly
(289.59) Other diseases of spleen
(289.6) Familial polycythemia
(289.7) Methemoglobinemia
(289.8) Other specified diseases of blood and blood-forming organs
(289.81) Primary hypercoagulable state
(289.82) Secondary hypercoagulable state
(289.83) Myelofibrosis
(289.84) Heparin-induced thrombocytopenia
(289.89) Other specified diseases of blood and blood-forming organs
(289.9) Unspecified diseases of blood and blood-forming organs