Classification of diseases and injuries



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4. DISEASES OF THE BLOOD AND BLOOD-FORMING ORGANS (280-289)

280 Iron deficiency anemias

Includes: anemia:

asiderotic

hypochromic-microcytic

sideropenic

Excludes: familial microcytic anemia (282.49)

280.0 Secondary to blood loss (chronic)

Normocytic anemia due to blood loss

Excludes: acute posthemorrhagic anemia (285.1)

280.1 Secondary to inadequate dietary iron intake

280.8 Other specified iron deficiency anemias

Paterson-Kelly syndrome

Plummer-Vinson syndrome

Sideropenic dysphagia

280.9 Iron deficiency anemia, unspecified

Anemia:

achlorhydric



chlorotic

idiopathic hypochromic

iron [Fe] deficiency NOS

281 Other deficiency anemias

281.0 Pernicious anemia

Anemia:


Addison's

Biermer's

congenital pernicious

Congenital intrinsic factor [Castle's] deficiency

Excludes: combined system disease without mention of anemia (266.2)

subacute degeneration of spinal cord without mention of anemia (266.2)

281.1 Other vitamin B12 deficiency anemia

Anemia:


vegan's

vitamin B12 deficiency (dietary)

due to selective vitamin B12 malabsorption with proteinuria

Syndrome:

Imerslund's

Imerslund-Gräsbeck

Excludes: combined system disease without mention of anemia (266.2)

subacute degeneration of spinal cord without mention of anemia (266.2)

281.2 Folate-deficiency anemia

Congenital folate malabsorption

Folate or folic acid deficiency anemia:

NOS


dietary

drug-induced

Goat's milk anemia

Nutritional megaloblastic anemia (of infancy)

Use additional E code to identify drug

281.3 Other specified megaloblastic anemias, not elsewhere classified

Combined B12 and folate-deficiency anemia

281.4 Protein-deficiency anemia

Amino-acid-deficiency anemia

281.8 Anemia associated with other specified nutritional deficiency

Scorbutic anemia

281.9 Unspecified deficiency anemia

Anemia:

dimorphic



macrocytic

megaloblastic NOS

nutritional NOS

simple chronic

282 Hereditary hemolytic anemias

282.0 Hereditary spherocytosis

Acholuric (familial) jaundice

Congenital hemolytic anemia (spherocytic)

Congenital spherocytosis

Minkowski-Chauffard syndrome

Spherocytosis (familial)

Excludes: hemolytic anemia of newborn (773.0-773.5)

282.1 Hereditary elliptocytosis

Elliptocytosis (congenital)

Ovalocytosis (congenital) (hereditary)

282.2 Anemias due to disorders of glutathione metabolism

Anemia:

6-phosphogluconic dehydrogenase deficiency



enzyme deficiency, drug-induced

erythrocytic glutathione deficiency

glucose-6-phosphate dehydrogenase [G-6-PD] deficiency

glutathione-reductase deficiency

hemolytic nonspherocytic (hereditary), type I

Disorder of pentose phosphate pathway

Favism

282.3 Other hemolytic anemias due to enzyme deficiency



Anemia:

hemolytic nonspherocytic (hereditary), type II

hexokinase deficiency

pyruvate kinase [PK] deficiency

triosephosphate isomerase deficiency

282.4 Thalassemias

Excludes: sickle-cell:

disease (282.60-282.69)

trait (282.5)

282.40 Thalassemia, unspecified

Thalassemia NOS

282.41 Sickle-cell thalassemia without crisis

Microdrepanocytosis

Sickle-cell thalassemia NOS

Thalassemia Hb-S disease without crisis

282.42 Sickle-cell thalassemia with crisis

Sickle-cell thalassemia with vaso-occlusive pain

Thalassemia Hb-S disease with crisis

Use additional code for type of crisis, such as:

Acute chest syndrome (517.3)

Splenic sequestration (289.52)

282.43 Alpha thalassemia

Alpha thalassemia major

Hemoglobin H Constant Spring

Hemoglobin H disease

Hydrops fetalis due to alpha thalassemia

Severe alpha thalassemia

Triple gene defect alpha thalassemia

Excludes: alpha thalassemia trait or minor (282.46)

hydrops fetalis due to isoimmunization (773.3)

hydrops fetalis not due to immune hemolysis (778.0)

282.44 Beta thalassemia

Beta thalassemia major

Cooley's anemia

Homozygous beta thalassemia

Severe beta thalassemia

Thalassemia intermedia

Thalassemia major

Excludes: beta thalassemia minor (282.46)

beta thalassemia trait (282.46)

delta-beta thalassemia (282.45)

hemoglobin E beta thalassemia (282.47)

sickle-cell beta thalassemia (282.41, 282.42)

282.45 Delta-beta thalassemia

Homozygous delta-beta thalassemia

Excludes: delta-beta thalassemia trait (282.46)

282.46 Thalassemia minor

Alpha thalassemia minor

Alpha thalassemia silent carrier

Alpha thalassemia trait

Beta thalassemia minor

Beta thalassemia trait

Delta-beta thalassemia trait

Thalassemia trait NOS

Excludes: alpha thalassemia (282.43)

beta thalassemia (282.44)

delta-beta thalassemia (282.45)

hemoglobin E-beta thalassemia (282.47)

sickle-cell trait (282.5)

282.47 Hemoglobin E-beta thalassemia

Excludes: beta thalassemia (282.44)

beta thalassemia minor (282.46)

beta thalassemia trait (282.46)

delta-beta thalassemia (282.45)

delta-beta thalassemia trait (282.46)

hemoglobin E disease (282.7)

other hemoglobinopathies (282.7)

sickle-cell beta thalassemia (282.41, 282.42)

282.49 Other thalassemia

Dominant thalassemia

Hemoglobin C thalassemia

Hereditary leptocytosis

Mediterranean anemia (with other hemoglobinopathy)

Mixed thalassemia

Thalassemia with other hemoglobinopathy

Excludes: hemoglobin C disease (282.7)

hemoglobin E disease (282.7)

other hemoglobinopathies (282.7)

sickle-cell anemias (282.60-282.69)

sickle-cell beta thalassemia (282.41-282.42)

282.5 Sickle-cell trait

Hb-AS genotype

Hemoglobin S [Hb-S] trait

Heterozygous:

hemoglobin S

Hb-S


Excludes: that with other hemoglobinopathy (282.60-282.69)

that with thalassemia (282.41-282.42)

282.6 Sickle-cell disease

Sickle-cell anemia

Excludes: sickle-cell thalassemia (282.41-282.42)

sickle-cell trait (282.5)

282.60 Sickle-cell disease, unspecified

Sickle-cell anemia NOS

282.61 Hb-SS disease without crisis

282.62 Hb-SS disease with crisis

Hb-SS disease with vaso-occlusive pain

Sickle-cell crisis NOS

Use additional code for type of crisis, such as:

Acute chest syndrome (517.3)

Splenic sequestration (289.52)

282.63 Sickle-cell/Hb-C disease without crisis

Hb-S/Hb-C disease without crisis

282.64 Sickle-cell/HB-C disease with crisis

Hb-S/Hb-C disease with crisis

Sickle-cell/Hb-C disease with vaso-occlusive pain

Use additional code for types of crisis, such as:

Acute chest syndrome (517.3)

Splenic sequestration (289.52)

282.68 Other sickle-cell disease without crisis

Hb-S/Hb-D disease without crisis

Hb-S/Hb-E disease without crisis

Sickle-cell/Hb-D disease without crisis

Sickle-cell/Hb-E disease without crisis

282.69 Other sickle-cell disease with crisis

Hb-S/Hb-D disease with crisis

Hb-S/Hb-E disease with crisis

Sickle-cell/Hb-D disease with crisis

Sickle-cell/Hb-E disease with crisis

Other sickle-cell disease with vaso-occlusive pain

Use additional code for type of crisis, such as:

Acute chest syndrome (517.3)

Splenic sequestration (289.52)

282.7 Other hemoglobinopathies

Abnormal hemoglobin NOS

Congenital Heinz-body anemia

Disease:

hemoglobin C [Hb-C]

hemoglobin D [Hb-D]

hemoglobin E [Hb-E]

hemoglobin Zurich [Hb-Zurich]

Hemoglobinopathy NOS

Hereditary persistence of fetal hemoglobin [HPFH]

Unstable hemoglobin hemolytic disease

Excludes: familial polycythemia (289.6)

hemoglobin E-beta thalassemia (282.47)

hemoglobin M [Hb-M] disease (289.7)

high-oxygen-affinity hemoglobin (289.0)

other hemoglobinopathies with thalassemia (282.49)

282.8 Other specified hereditary hemolytic anemias

Stomatocytosis

282.9 Hereditary hemolytic anemia, unspecified

Hereditary hemolytic anemia NOS

283 Acquired hemolytic anemias

283.0 Autoimmune hemolytic anemias

Autoimmune hemolytic disease (cold type) (warm type)

Chronic cold hemagglutinin disease

Cold agglutinin disease or hemoglobinuria

Hemolytic anemia:

cold type (secondary) (symptomatic)

drug-induced

warm type (secondary) (symptomatic)

Use additional E code to identify cause, if drug-induced

Excludes: Evans' syndrome (287.32)

hemolytic disease of newborn (773.0-773.5)

283.1 Non-autoimmune hemolytic anemias

283.10 Non-autoimmune hemolytic anemia, unspecified

283.11 Hemolytic-uremic syndrome

Use additional code to identify associated:

E. coli infection (041.41-041.49)

Pneumococcal pnemonia (481)

Shigella dysenteriae (004.0)

283.19 Other non-autoimmune hemolytic anemias

Hemolytic anemia:

mechanical

microangiopathic

toxic

Use additional E code to identify cause



283.2 Hemoglobinuria due to hemolysis from external causes

Acute intravascular hemolysis

Hemoglobinuria:

from exertion

march

paroxysmal (cold) (nocturnal)



due to other hemolysis

Marchiafava-Micheli syndrome

Use additional E code to identify cause

283.9 Acquired hemolytic anemia, unspecified

Acquired hemolytic anemia NOS

Chronic idiopathic hemolytic anemia

284 Aplastic anemia and other bone marrow failure syndromes

284.0 Constitutional aplastic anemia

284.01 Constitutional red blood cell aplasia

Aplasia, (pure) red cell:

congenital

of infants

primary

Blackfan-Diamond syndrome



Familial hypoplastic anemia

284.09 Other constitutional aplastic anemia

Fanconi's anemia

Pancytopenia with malformations

284.1 Pancytopenia

Excludes: pancytopenia (due to) (with):

aplastic anemia NOS (284.9)

bone marrow infiltration (284.2)

constitutional red blood cell aplasia (284.01)

hairy cell leukemia (202.4)

human immunodeficiency virus disease (042)

leukoerythroblastic anemia (284.2)

malformations (284.09)

myelodysplastic syndromes (238.72-238.75)

myeloproliferative disease (238.79)

other constitutional aplastic anemia (284.09)

284.11 Antineoplastic chemotherapy induced pancytopenia

Excludes: aplastic anemia due to antineoplastic chemotherapy (284.89)

284.12 Other drug-induced pancytopenia

Excludes: aplastic anemia due to drugs (284.89)

284.19 Other pancytopenia

284.2 Myelophthisis

Leukoerythroblastic anemia

Myelophthisic anemia

Code firstthe underlying disorder, such as:

malignant neoplasm of breast (174.0-174.9, 175.0-175.9)

tuberculosis (015.0-015.9)

Excludes: idiopathic myelofibrosis (238.76)

myelofibrosis NOS (289.83)

myelofibrosis with myeloid metaplasia (238.76)

primary myelofibrosis (238.76)

secondary myelofibrosis (289.83)

284.8 Other specified aplastic anemias

284.81 Red cell aplasia (acquired) (adult) (with thymoma)

Red cell aplasia NOS

284.89 Other specified aplastic anemias

Aplastic anemia (due to):

chronic systemic disease

drugs

infection



radiation

toxic (paralytic)

Use additional E code to identify cause

284.9 Aplastic anemia, unspecified

Anemia:

aplastic (idiopathic) NOS



aregenerative

hypoplastic NOS

nonregenerative

Medullary hypoplasia

Excludes: refractory anemia (238.72)

285 Other and unspecified anemias

285.0 Sideroblastic anemia

Anemia:


hypochromic with iron loading

sideroachrestic

sideroblastic:

acquired


congenital

hereditary

primary

secondary (drug-induced) (due to disease)



sex-linked hypochromic

vitamin B6-responsive

Pyridoxine-responsive (hypochromic) anemia

Excludes: refractory sideroblastic anemia (238.72)

Use additional E code to identify cause, if drug-induced

285.1 Acute posthemorrhagic anemia

Anemia due to acute blood loss

Excludes: anemia due to chronic blood loss (280.0)

blood loss anemia NOS (280.0)

285.2 Anemia of chronic disease

Anemia in (due to) (with) chronic illness

285.21 Anemia in chronic kidney disease

Anemia in end-stage renal disease

Erythropoietin-resistant anemia (EPO resistant anemia)

285.22 Anemia in neoplastic disease

Excludes: anemia due to antineoplastic chemotherapy (285.3)

aplastic anemia due to antineoplastic chemotherapy (284.89)

285.29 Anemia of other chronic disease

Anemia in other chronic illness

285.3 Antineoplastic chemotherapy induced anemia

Anemia due to antineoplastic chemotherapy

Excludes: anemia due to drug NEC - code to type of anemia

anemia in neoplastic disease (285.22)

aplastic anemia due to antineoplastic chemotherapy (284.89)

285.8 Other specified anemias

Anemia:


dyserythropoietic (congenital)

dyshematopoietic (congenital)

von Jaksch's

Infantile pseudoleukemia

285.9 Anemia, unspecified

Anemia:


NOS

essential

normocytic, not due to blood loss

profound


progressive

secondary

Oligocythemia

Excludes: anemia (due to):

blood loss:

acute (285.1)

chronic or unspecified (280.0)

iron deficiency (280.0-280.9)

286 Coagulation defects

286.0 Congenital factor VIII disorder

Antihemophilic globulin [AHG] deficiency

Factor VIII (functional) deficiency

Hemophilia:

NOS


A

classical

familial

hereditary

Subhemophilia

Excludes: factor VIII deficiency with vascular defect (286.4)

286.1 Congenital factor IX disorder

Christmas disease

Deficiency:

factor IX (functional)

plasma thromboplastin component [PTC]

Hemophilia B

286.2 Congenital factor XI deficiency

Hemophilia C

Plasma thromboplastin antecedent [PTA] deficiency

Rosenthal's disease

286.3 Congenital deficiency of other clotting factors

Congenital afibrinogenemia

Deficiency:

AC globulin

factor:

I [fibrinogen]



II [prothrombin]

V [labile]

VII [stable]

X [Stuart-Prower]

XII [Hageman]

XIII [fibrin stabilizing]

Laki-Lorand factor

proaccelerin

Disease:

Owren's


Stuart-Prower

Dysfibrinogenemia (congenital)

Dysprothrombinemia (constitutional)

Hypoproconvertinemia

Hypoprothrombinemia (hereditary)

Parahemophilia

286.4 von Willebrand's disease

Angiohemophilia (A) (B)

Constitutional thrombopathy

Factor VIII deficiency with vascular defect

Pseudohemophilia type B

Vascular hemophilia

von Willebrand's (-Jürgens') disease

Excludes: factor VIII deficiency:

NOS (286.0)

with functional defect (286.0)

hereditary capillary fragility (287.8)

286.5 Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors

286.52 Acquired hemophilia

Autoimmune hemophilia

Autoimmune inhibitors to clotting factors

Secondary hemophilia

286.53 Antiphospholipid antibody with hemorrhagic disorder

Lupus anticoagulant (LAC) with hemorrhagic disorder

Systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder

Excludes: antiphospholipid antibody, finding without diagnosis (795.79)

antiphospholipid antibody syndrome (289.81)

antiphospholipid antibody with hypercoagulable state (289.81)

lupus anticoagulant (LAC) finding without diagnosis (795.79)

lupus anticoagulant (LAC) with hypercoagulable state (289.81)

systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (795.79)

systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (289.81)

286.59 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors

Antithrombinemia

Antithromboplastinemia

Antithromboplastinogenemia

Increase in:

anti-II (prothrombin)

anti-VIIIa

anti-IXa


anti-Xla

286.6 Defibrination syndrome

Afibrinogenemia, acquired

Consumption coagulopathy

Diffuse or disseminated intravascular coagulation [DIC syndrome]

Fibrinolytic hemorrhage, acquired

Hemorrhagic fibrinogenolysis

Pathologic fibrinolysis

Purpura:

fibrinolytic

fulminans

Excludes: that complicating:

abortion (634-638 with.1, 639.1)

pregnancy or the puerperium (641.3, 666.3)

disseminated intravascular coagulation in newborn (776.2)

286.7 Acquired coagulation factor deficiency

Deficiency of coagulation factor due to:

liver disease

vitamin K deficiency

Hypoprothrombinemia, acquired

Excludes: vitamin K deficiency of newborn (776.0)

Use additional E-code to identify cause, if drug-induced

286.9 Other and unspecified coagulation defects

Defective coagulation NOS

Deficiency, coagulation factor NOS

Delay, coagulation

Disorder:

coagulation

hemostasis

Excludes: abnormal coagulation profile (790.92)

hemorrhagic disease of newborn (776.0)

that complicating:

abortion (634-638 with.1, 639.1)

pregnancy or the puerperium (641.3, 666.3)

287 Purpura and other hemorrhagic conditions

Excludes: hemorrhagic thrombocythemia (238.79)

purpura fulminans (286.6)

287.0 Allergic purpura

Peliosis rheumatica

Purpura:


anaphylactoid

autoimmune

Henoch's

nonthrombocytopenic:

hemorrhagic

idiopathic

rheumatica

Schönlein-Henoch

vascular

Vasculitis, allergic

Excludes: hemorrhagic purpura (287.39)

purpura annularis telangiectodes (709.1)

287.1 Qualitative platelet defects

Thrombasthenia (hemorrhagic) (hereditary)

Thrombocytasthenia

Thrombocytopathy (dystrophic)

Thrombopathy (Bernard-Soulier)

Excludes: von Willebrand's disease (286.4)

287.2 Other nonthrombocytopenic purpuras

Purpura:


NOS

senile


simplex

287.3 Primary thrombocytopenia

Excludes: thrombotic thrombocytopenic purpura (446.6)

transient thrombocytopenia of newborn (776.1)

287.30 Primary thrombocytopenia unspecified

Megakaryocytic hypoplasia

287.31 Immune thrombocytopenic purpura

Idiopathic thrombocytopenic purpura

Tidal platelet dysgenesis

287.32 Evans' syndrome

287.33 Congenital and hereditary thrombocytopenic purpura

Congenital and hereditary thrombocytopenia

Thrombocytopenia with absent radii (TAR) syndrome

Excludes: Wiskott-Aldrich syndrome (279.12)

287.39 Other primary thrombocytopenia

287.4 Secondary thrombocytopenia

Use additional E code to identify cause

Excludes: heparin-induced thrombocytopenia (HIT) (289.84)

transient thrombocytopenia of newborn (776.1)

287.41 Posttransfusion purpura

Posttransfusion purpura from whole blood (fresh) or blood products

PTP


287.49 Other secondary thrombocytopenia

Thrombocytopenia (due to):

dilutional

drugs


extracorporeal circulation of blood

massive blood transfusion

platelet alloimmunization

secondary NOS

287.5 Thrombocytopenia, unspecified

287.8 Other specified hemorrhagic conditions

Capillary fragility (hereditary)

Vascular pseudohemophilia

287.9 Unspecified hemorrhagic conditions

Hemorrhagic diathesis (familial)

288 Diseases of white blood cells

Excludes: leukemia (204.0-208.9)

288.0 Neutropenia

Decreased Absolute Neutrophil Count (ANC)

Use additional code for any associated:

fever (780.61)

mucositis (478.11, 528.00-528.09, 538, 616.81)

Excludes: neutropenic splenomegaly (289.53)

transitory neonatal neutropenia (776.7)

288.00 Neutropenia, unspecified

288.01 Congenital neutropenia

Congenital agranulocytosis

Infantile genetic agranulocytosis

Kostmann's syndrome

288.02 Cyclic neutropenia

Cyclic hematopoiesis

Periodic neutropenia

288.03 Drug induced neutropenia

Use additional E code to identify drug

288.04 Neutropenia due to infection

288.09 Other neutropenia

Agranulocytosis

Neutropenia:

immune


toxic

288.1 Functional disorders of polymorphonuclear neutrophils

Chronic (childhood) granulomatous disease

Congenital dysphagocytosis

Job's syndrome

Lipochrome histiocytosis (familial)

Progressive septic granulomatosis

288.2 Genetic anomalies of leukocytes

Anomaly (granulation) (granulocyte) or syndrome:

Alder's (-Reilly)

Chédiak-Steinbrinck (-Higashi)

Jordan's


May-Hegglin

Pelger-Huet

Hereditary:

hypersegmentation

hyposegmentation

leukomelanopathy

288.3 Eosinophilia

Eosinophilia

allergic

hereditary

idiopathic

secondary

Eosinophilic leukocytosis

Excludes: Löffler's syndrome (518.3)

pulmonary eosinophilia (518.3)

288.4 Hemophagocytic syndromes

Familial hemophagocytic lymphohistiocytosis

Familial hemophagocytic reticulosis

Hemophagocytic syndrome, infection-associated

Histiocytic syndromes

Macrophage activation syndrome

288.5 Decreased white blood cell count

Excludes: neutropenia (288.01-288.09)

288.50 Leukocytopenia, unspecified

Decreased leukocytes, unspecified

Decreased white blood cell count, unspecified

Leukopenia NOS

288.51 Lymphocytopenia

Decreased lymphocytes

288.59 Other decreased white blood cell count

Basophilic leukopenia

Eosinophilic leukopenia

Monocytopenia

Plasmacytopenia

288.6 Elevated white blood cell count

Excludes: eosinophilia (288.3)

288.60 Leukocytosis, unspecified

Elevated leukocytes, unspecified

Elevated white blood cell count, unspecified

288.61 Lymphocytosis (symptomatic)

Elevated lymphocytes

288.62 Leukemoid reaction

Basophilic leukemoid reaction

Lymphocytic leukemoid reaction

Monocytic leukemoid reaction

Myelocytic leukemoid reaction

Neutrophilic leukemoid reaction

288.63 Monocytosis (symptomatic)

Excludes: infectious mononucleosis (075)

288.64 Plasmacytosis

288.65 Basophilia

288.66 Bandemia

Bandemia without diagnosis of specific infection

Excludes: confirmed infection - code to infection

leukemia (204.00-208.9)

288.69 Other elevated white blood cell count

288.8 Other specified disease of white blood cells

Excludes: decreased white blood cell counts (288.50-288.59)

elevated white blood cell counts (288.60-288.69)

immunity disorders (279.0-279.9)

288.9 Unspecified disease of white blood cells

289 Other diseases of blood and blood-forming organs

289.0 Polycythemia, secondary

High-oxygen-affinity hemoglobin

Polycythemia:

acquired


benign

due to:


fall in plasma volume

high altitude

emotional

erythropoietin

hypoxemic

nephrogenous

relative

spurious


stress

Excludes: polycythemia:

neonatal (776.4)

primary (238.4)

vera (238.4)

289.1 Chronic lymphadenitis

Chronic:

adenitis any lymph node, except mesenteric

lymphadenitis any lymph node, except mesenteric

Excludes: acute lymphadenitis (683)

mesenteric (289.2)

enlarged glands NOS (785.6)

289.2 Nonspecific mesenteric lymphadenitis

Mesenteric lymphadenitis (acute) (chronic)

289.3 Lymphadenitis, unspecified, except mesenteric

289.4 Hypersplenism

"Big spleen" syndrome

Dyssplenism

Hypersplenia

Excludes: primary splenic neutropenia (289.53)

289.5 Other diseases of spleen

289.50 Disease of spleen, unspecified

289.51 Chronic congestive splenomegaly

289.52 Splenic sequestration

Code firstsickle-cell disease in crisis (282.42, 282.62, 282.64, 282.69)

289.53 Neutropenic splenomegaly

289.59 Other

Lien migrans

Perisplenitis

Splenic:


abscess

atrophy


cyst

fibrosis


infarction

rupture, nontraumatic

Splenitis

Wandering spleen

Excludes: bilharzial splenic fibrosis (120.0-120.9)

hepatolienal fibrosis (571.5)

splenomegaly NOS (789.2)

289.6 Familial polycythemia

Familial:

benign polycythemia

erythrocytosis

289.7 Methemoglobinemia

Congenital NADH [DPNH]-methemoglobin-reductase deficiency

Hemoglobin M [Hb-M] disease

Methemoglobinemia:

NOS


acquired (with sulfhemoglobinemia)

hereditary

toxic

Stokvis' disease



Sulfhemoglobinemia

Use additional E code to identify cause

289.8 Other specified diseases of blood and blood-forming organs

289.81 Primary hypercoagulable state

Activated protein C resistance

Antiphospholipid antibody syndrome

Antithrombin III deficiency

Factor V Leiden mutation

Lupus anticoagulant with hypercoagulable state

Protein C deficiency

Protein S deficiency

Prothrombin gene mutation

Systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state

Excludes: anti-phospholipid antibody, finding without diagnosis (795.79)

anti-phospholipid antibody with hemorrhagic disorder (286.53)

lupus anticoagulant (LAC) finding without diagnosis (795.79)

lupus anticoagulant (LAC) with hemorrhagic disorder (286.53)

secondary activated protein C resistance (289.82)

secondary antiphospholipid antibody syndrome (289.82)

secondary lupus anticoagulant with hypercoagulable state (289.82)

secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (289.82)

systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (795.79)

systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (286.53)

289.82 Secondary hypercoagulable state

Excludes: heparin-induced thrombocytopenia (HIT) (289.84)

289.83 Myelofibrosis

Myelofibrosis NOS

Secondary myelofibrosis

Code first the underlying disorder, such as:

malignant neoplasm of breast (174.0-174.9, 175.0-175.9)

Use additional code for associated therapy-related myelodysplastic syndrome, if applicable (238.72, 238.73)

Use additional external cause code if due to anti-neoplastic chemotherapy (E933.1)

Excludes: idiopathic myelofibrosis (238.76)

leukoerythroblastic anemia (284.2)

myelofibrosis with myeloid metaplasia (238.76)

myelophthisic anemia (284.2)

myelophthisis (284.2)

primary myelofibrosis (238.76)

289.84 Heparin-induced thrombocytopenia (HIT)

289.89 Other specified diseases of blood and blood-forming organs

Hypergammaglobulinemia

Pseudocholinesterase deficiency

289.9 Unspecified diseases of blood and blood-forming organs

Blood dyscrasia NOS

Erythroid hyperplasia

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