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C00-D48 - Neoplasms

see now ICD-10 Chapter II: Neoplasms

D50-D89 - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

(D50-D53) Nutritional anemias

(D50.) Iron deficiency anaemia
- (D 50.0) Iron deficiency anaemia secondary to blood loss (chronic)
- (D50.1) Sideropenic dysphagia
  - Kelly-Paterson syndrome
  - Plummer-Vinson syndrome
- (D 50.8) Other iron deficiency anaemias
- (D 50.9) Iron deficiency anaemia, unspecified

(D51.) Vitamin B12 deficiency anaemia
- (D51.0) Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
  - Pernicious anemia
- (D51.1) Vitamin B 12 deficiency anaemia due to selective vitamin B 12 malabsorption with proteinuria
  - Megaloblastic hereditary anaemia
- (D 51.2) Transcobalamin II deficiency
- (D 51.3) Other dietary vitamin B 12 deficiency anaemia
- (D 51.8) Other vitamin B 12 deficiency anaemias
- (D 51.9) Vitamin B 12 deficiency anaemia, unspecified

(D52.) Folate deficiency anaemia
- (D52.0) Dietary folate deficiency anaemia
  - Nutritional megaloblastic anaemia
- (D 52.1) Drug-induced folate deficiency anaemia
- (D 52.8) Other folate deficiency anaemias
- (D 52.9) Folate deficiency anaemia, unspecified

(D53.) Other nutritional anaemias
- (D 53.0) Protein deficiency anaemia
- (D 53.1) Other megaloblastic anaemias, not elsewhere classified
- (D 53.2) Scorbutic anaemia
- (D 53.8) Other specified nutritional anaemias
- (D 53.9) Nutritional anaemia, unspecified

(D55-D59) Haemolytic anaemias

(D55.) Anaemia due to enzyme disorders
- (D55.0) Anaemia due to glucose-6-phosphate dehydrogenase (G6PD) deficiency
  - Favism
  - G6PD deficiency anaemia
- (D 55.1) Anaemia due to other disorders of glutathione metabolism
- (D 55.2) Anaemia due to disorders of glycolytic enzymes
- (D 55.3) Anaemia due to disorders of nucleotide metabolism
- (D 55.8) Other anaemias due to enzyme disorders
- (D 55.9) Anaemia due to enzyme disorder, unspecified

(D56.) Thalassaemia
- (D 56.0) Alpha thalassaemia
- (D 56.1) Beta thalassaemia
- (D 56.2) Delta-beta thalassaemia
- (D 56.3) Thalassaemia trait
- (D 56.4) Hereditary persistence of fetal haemoglobin (HPFH)
- (D 56.8) Other thalassaemias
- (D 56.9) Thalassaemia, unspecified

(D57.) Sickle-cell disorders
- (D 57.0) Sickle-cell anaemia with crisis
- (D 57.1) Sickle-cell anaemia without crisis
- (D 57.2) Double heterozygous sickling disorders
- (D 57.3) Sickle-cell trait
- (D 57.8) Other sickle-cell disorders

(D58.) Other hereditary haemolytic anaemias
- (D58.0) Hereditary spherocytosis
- (D58.1) Hereditary elliptocytosis
  - Elliptocytosis (congenital)
  - Ovalocytosis (congenital)(hereditary)
- (D58.2) Other haemoglobinopathies
- (D58.8) Other specified hereditary haemolytic anaemias
  - Stomatocytosis

(D59.) Acquired haemolytic anaemia
- (D 59.0) Drug-induced autoimmune haemolytic anaemia
- (D59.1) Other autoimmune haemolytic anaemias
  - Warm autoimmune hemolytic anemia
- (D 59.2) Drug-induced nonautoimmune haemolytic anaemia
- (D 59.3) Haemolytic-uraemic syndrome
- (D59.4) Other nonautoimmune haemolytic anaemias
  - Microangiopathic hemolytic anemia
- (D 59.5) Paroxysmal nocturnal haemoglobinuria (Marchiafava-Micheli)
- (D59.6) Haemoglobinuria due to haemolysis from other external causes
  - paroxysmal cold haemoglobinuria
- (D 59.8) Other acquired haemolytic anaemias
- (D 59.9) Acquired haemolytic anaemia, unspecified

(D 77.) Other disorders of blood and blood-forming organs in diseases classified elsewhere

(D80-D89) Certain disorders involving the immune mechanism

(D80.) Immunodeficiency with predominantly antibody defects
- (D80.0) Hereditary hypogammaglobulinaemia
  - Autosomal recessive agammaglobulinaemia (Swiss type)
  - X-linked agammaglobulinaemia (Bruton) (with growth hormone deficiency)
- (D80.1) Nonfamilial hypogammaglobulinaemia
- (D 80.2) Selective deficiency of immunoglobulin A (IgA)
- (D 80.3) Selective deficiency of immunoglobulin G (IgG) subclasses
- (D 80.4) Selective deficiency of immunoglobulin M (IgM)
- (D 80.5) Immunodeficiency with increased immunoglobulin M (IgM)
- (D 80.6) Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
- (D 80.7) Transient hypogammaglobulinaemia of infancy
- (D80.8) Other immunodeficiencies with predominantly antibody defects
  - Kappa light chain deficiency
- (D 80.8) Immunodeficiency with predominantly antibody defects, unspecified

(D81.) Combined immunodeficiencies
- (D 81.0) Severe combined immunodeficiency (SCID) with reticular dysgenesis
- (D 81.1) Severe combined immunodeficiency (SCID) with low T-cell and B-cell numbers
- (D 81.2) Severe combined immunodeficiency (SCID) with low or normal B-cell numbers
- (D 81.3) Adenosine deaminase deficiency (ADA)
- (D 81.4) Nezelof\'s syndrome
- (D 81.5) Purine nucleoside phosphorylase deficiency (PNP)
- (D81.6) Major histocompatibility complex class I deficiency
  - Bare lymphocyte syndrome
- (D 81.7) Major histocompatibility complex class II deficiency
- (D81.8) Other combined immunodeficiencies
  - Biotin-dependent carboxylase deficiency
- (D81.9) Combined immunodeficiency, unspecified
  - Severe combined immunodeficiency disorder (SCID) NOS

(D82.) Immunodeficiency associated with other major defects
- (D82.0) Wiskott-Aldrich syndrome
  - Immunodeficiency with thrombocytopenia and eczema
- (D 82.1) Di George\'s syndrome
- (D 82.2) Immunodeficiency with short-limbed stature
- (D82.3) Immunodeficiency following hereditary defective response to Epstein-Barr virus
  - X-linked lymphoproliferative disease
- (D 82.4) Hyperimmunoglobulin E syndrome (IgE)
(D 83.) Common variable immunodeficiency

(D84.) Other immunodeficiencies
- (D 84.0) Lymphocyte function antigen-1 (LFA-1) defect
- (D84.1) Defects in the complement system
  - C1 esterase inhibitor deficiency (C1-INH)
- (D 84.8) Other specified immunodeficiencies
- (D 84.9) Immunodeficiency, unspecified

(D86.) Sarcoidosis
- (D 86.0) Sarcoidosis of lung
- (D 86.1) Sarcoidosis of lymph nodes
- (D 86.2) Sarcoidosis of lung with sarcoidosis of lymph nodes
- (D 86.3) Sarcoidosis of skin
- (D 86.8) Sarcoidosis of other and combined sites
(D89.) Other disorders involving the immune mechanism, not elsewhere classified
- (D89.0) Polyclonal hypergammaglobulinaemia
  - Benign hypergammaglobulinaemic purpura
  - Polyclonal gammopathy NOS
- (D 89.1) Cryoglobulinaemia
- (D 89.2) Hypergammaglobulinaemia, unspecified
- (D 89.8) Other specified disorders involving the immune mechanism, not elsewhere classified
- (D 89.9) Disorder involving the immune mechanism, unspecified

v • d • e Pathology: Cancer, Tumors, Neoplasms, and oncology (C00-D48, 140-239)
Benign tumors	Hyperplasia - Cyst - Pseudocyst - Hamartoma - Benign tumor
Malignant progression	Dysplasia - Carcinoma in situ - Cancer - Metastasis
Topography	lip, oral cavity and pharynx: Oral - Head/Neck - Nasopharyngeal digestive system: tract (Esophagus, Stomach, Small intestine, Colon/rectum, Appendix, Anus) - glands (Liver, Bile duct, Gallbladder, Pancreas) respiratory system: Larynx - Lung bone, articular cartilage, skin, and connective tissue: Bone - Skin - Blood urogenital: breast and female genital organs (Breast, Vagina, Cervix, Uterus, Endometrium, Ovaries) - male genital organs (Penis, Prostate, Testicles) - urinary organs (Kidney, Bladder) nervous system: Eye (Uvea) - Brain endocrine system: Thyroid (Papillary, Follicular, Medullary, Anaplastic) - Adrenal tumor (Adrenocortical carcinoma, Pheochromocytoma) - Pituitary
Misc.	Tumor suppressor genes/oncogenes - Staging/grading - Carcinogenesis - Carcinogen - Research - Paraneoplastic syndrome - List of oncology-related terms

v • d • e Pathology: hematology (primarily D50-D77, 280-289)
RBCs/anemia/ hemoglobinopathy (Myeloid)	nutritional anemia: Iron deficiency anemia, Plummer-Vinson syndrome, Megaloblastic anemia (Pernicious anemia) hereditary hemolytic anemia: G6PD Deficiency, Thalassemia, Sickle-cell disease/trait, Hereditary spherocytosis, Hereditary elliptocytosis, Hereditary stomatocytosis acquired hemolytic anemia: Autoimmune (Warm), HUS, MAHA, PNH, PCH aplastic anemia: Acquired PRCA, Diamond-Blackfan anemia, Fanconi anemia • Sideroblastic anemia • Hemochromatosis
Coagulation/platelets (Myeloid)	coagulopathy: DIC (Congenital afibrinogenemia, Purpura fulminans) • Hemophilia (A/VII, B/IX, C/XI, XIII) • Von Willebrand disease Purpura: Henoch-Schönlein, ITP (Evans syndrome), TTP primary hypercoagulable state: Protein C deficiency - Protein S deficiency - Antithrombin III deficiency - Factor V Leiden - Activated protein C resistance - Antiphospholipid syndrome other hemorrhagic conditions: Bernard-Soulier syndrome - Glanzmann\'s thrombasthenia - Grey platelet syndrome - May Hegglin anomaly Essential thrombocytosis - Thrombocytopenia
Monocytes/Macrophages (Myeloid)	WHO-I histiocytosis (Langerhans cell histiocytosis) WHO-II/non-Langerhans-cell histiocytosis (Juvenile xanthogranuloma, Hemophagocytic lymphohistiocytosis) WHO-III/malignant histiocytic disorders (Acute monocytic leukemia, Malignant histiocytosis, Erdheim-Chester disease) -cytosis: Monocytosis -penia: Monocytopenia
Granulocytes (Myeloid)	-cytosis: granulocytosis (Neutrophilia, Eosinophilia, Basophilia) -penia: Granulocytopenia/agranulocytosis (Neutropenia, Kostmann syndrome)
Other/general myeloid	Chronic granulomatous disease
Lymphoid	-cytosis: Lymphocytosis -penia: Lymphopenia
Other	Asplenia/hyposplenism - Methemoglobinemia - Pancytopenia
See also hematological malignancy and immune disorders

v • d • e

Pathology: Immune disorders (primarily D80-D89, 273, 279)

Immunodeficiency/
primary

Antibody/humoral (B)	Hypogammaglobulinemia/agammaglobulinemia (X-linked, Transient of infancy) - Dysgammaglobulinemia (IgA, IgG) - Leukocyte adhesion deficiency - Common variable immunodeficiency
Cell-mediated (T)	DiGeorge syndrome - Wiskott-Aldrich syndrome - Nezelof syndrome
Combined (B+T)	Severe combined immunodeficiency (Adenosine deaminase deficiency, Omenn syndrome, X-SCID, ZAP70 deficiency) - Purine nucleoside phosphorylase deficiency - Bare lymphocyte syndrome
Complement deficiency	Angioedema
PBD	Hyper-IgE syndrome - Chédiak-Higashi syndrome - Chronic granulomatous disease
Other	ICF syndrome

Immunoproliferative

Hypergammaglobulinemia - Paraproteinemia (Cryoglobulinemia, Heavy chain disease,

Icd-10_chapter_c

Contents

C00-D48 - Neoplasms

D50-D89 - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

(D50-D53) Nutritional anemias

(D55-D59) Haemolytic anaemias

(D60-D64) Aplastic and other anaemias

(D65-D69) Coagulation defects, purpura and other haemorrhagic conditions

(D70-D77) Other diseases of blood and blood-forming organs

(D80-D89) Certain disorders involving the immune mechanism

See also