(C95.) Leukaemia of unspecified cell type
- (C 95.0) Acute leukaemia of unspecified cell type
- (C 95.1) Chronic leukaemia of unspecified cell type
- (C 95.2) Subacute leukaemia of unspecified cell type
- (C 95.7) Other leukaemia of unspecified cell type
- (C 95.9) Leukaemia, unspecified

(C96.) Other and unspecified malignant neoplasms of lymphoid, haematopoietic and related tissue
- (C 96.0) Letterer-Siwe disease
- (C 96.1) Malignant histiocytosis
- (C 96.2) Malignant mast cell tumour
- (C 96.3) True histiocytic lymphoma
- (C 96.7) Other specified malignant neoplasms of lymphoid, haematopoietic and related tissue
- (C 96.9) Malignant neoplasm of lymphoid, haematopoietic and related tissue, unspecified

[edit] (C97) Malignant neoplasms of independent (primary) multiple sites

(C 97.) Malignant neoplasms of independent (primary) multiple sites

[edit] (D00-D09) In situ neoplasms

(D 00.) Carcinoma in situ of oral cavity, oesophagus and stomach
(D 01.) Carcinoma in situ of other and unspecified digestive organs
(D 02.) Carcinoma in situ of middle ear and respiratory system
(D 03.) Melanoma in situ
(D 04.) Carcinoma in situ of skin
(D 05.) Carcinoma in situ of breast
(D 06.) Carcinoma in situ of cervix uteri
(D 07.) Carcinoma in situ of other and unspecified genital organs
(D 09.) Carcinoma in situ of other and unspecified sites

[edit] (D10-D36) Benign neoplasms

(D 10.) Benign neoplasm of mouth and pharynx

(D11.) Benign neoplasm of major salivary glands
- Warthin's tumor
- Pleomorphic adenoma
- (D 11.0) Parotid gland
- (D11.7) Other major salivary glands
  - Sublingual gland
  - Submandibular gland
- (D 11.9) Major salivary gland, unspecified

(D12.) Benign neoplasm of colon, rectum, anus and anal canal
- Familial adenomatous polyposis
- (D 12.0) Caecum
- (D 12.1) Appendix
- (D 12.2) Ascending colon
- (D 12.3) Transverse colon
- (D 12.4) Descending colon
- (D 12.5) Sigmoid colon
- (D12.6) Colon, unspecified
  - Adenomatosis of colon
- (D 12.7) Rectosigmoid junction
- (D 12.8) Rectum
- (D 12.9) Anus and anal canal

(D13.) Benign neoplasm of other and ill-defined parts of digestive system
- (D 13.0) Oesophagus
- (D 13.1) Stomach
- (D 13.2) Duodenum
- (D 13.3) Other and unspecified parts of small intestine
- (D13.4) Liver
  - Intrahepatic bile ducts
- (D 13.5) Extrahepatic bile ducts
- (D 13.6) Pancreas
- (D13.7) Endocrine pancreas
  - Islet cell tumour
  - Islets of Langerhans
- (D13.9) Ill-defined sites within the digestive system
  - Digestive system NOS
  - Intestine NOS
  - Spleen

(D 14.) Benign neoplasm of middle ear and respiratory system

(D15.) Benign neoplasm of other and unspecified intrathoracic organs
- (D 15.0) Thymus
- (D15.1) Heart
  - Myxoma
- (D 15.2) Mediastinum

(D 16.) Benign neoplasm of bone and articular cartilage

(D17.) Benign lipomatous neoplasm
- Lipoma (ILDS D17.910)
- Lipomata, multiple (ILDS D17.920)
- Angiolipoma (ILDS D17.930)
- Lipoblastomatosis (ILDS D17.940)
- Hibernoma (ILDS D17.950)

(D18.) Haemangioma and lymphangioma, any site
- (D18.0) Haemangioma, any site
  - Angioma NOS
- (D18.1) Lymphangioma, any site
  - Cavernous haemangioma (ILDS D18.014)

(D 19.) Benign neoplasm of mesothelial tissue
(D 20.) Benign neoplasm of soft tissue of retroperitoneum and peritoneum
(D21.) Other benign neoplasms of connective and other soft tissue
- Chondroma
- Masson's pseudoangiosarcoma (ILDS D21.M20)
- Synovioma, giant-cell (ILDS D21.M30)
- Leiomyoma (ILDS D21.M40)
- Rhabdomyoma (ILDS D21.M50)
- Angioleiomyoma (ILDS D21.M60)

(D 22.) Melanocytic naevi

(D 23.) Other benign neoplasms of skin

(D 24.) Benign neoplasm of breast

(D25.) Leiomyoma of uterus
- Uterine fibroids

(D 26.) Other benign neoplasms of uterus

(D 27.) Benign neoplasm of ovary

(D 28.) Benign neoplasm of other and unspecified female genital organs

(D 29.) Benign neoplasm of male genital organs

(D 30.) Benign neoplasm of urinary organs

(D 31.) Benign neoplasm of eye and adnexa

(D 32.) Benign neoplasm of meninges

(D 33.) Benign neoplasm of brain and other parts of central nervous system

(D 34.) Benign neoplasm of thyroid gland

(D35.) Benign neoplasm of other and unspecified endocrine glands
- (D 35.0) Adrenal gland
- (D 35.1) Parathyroid gland
- (D35.2) Pituitary gland
  - Pituitary adenoma
  - Prolactinoma
- (D 35.3) Craniopharyngeal duct
- (D 35.4) Pineal gland
- (D 35.5) Carotid body
- (D 35.6) Aortic body and other paraganglia
- (D 35.7) Other specified endocrine glands
- (D 35.8) Pluriglandular involvement
- (D 35.9) Endocrine gland, unspecified

(D 36.) Benign neoplasm of other and unspecified sites

[edit] (D37-D48) Neoplasms of uncertain or unknown behaviour

(D 37.) Neoplasm of uncertain or unknown behaviour of oral cavity and digestive organs
(D 38.) Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs
(D 39.) Neoplasm of uncertain or unknown behaviour of female genital organs
(D 40.) Neoplasm of uncertain or unknown behaviour of male genital organs
(D 41.) Neoplasm of uncertain or unknown behaviour of urinary organs
(D 42.) Neoplasm of uncertain or unknown behaviour of meninges
(D 43.) Neoplasm of uncertain or unknown behaviour of brain and central nervous system

(D44.) Neoplasm of uncertain or unknown behaviour of endocrine glands
- (D 44.0) Thyroid gland
- (D 44.1) Adrenal gland
- (D 44.2) Parathyroid gland
- (D 44.3) Pituitary gland
- (D 44.4) Craniopharyngeal duct
- (D 44.5) Pineal gland
- (D 44.6) Carotid body
- (D 44.7) Aortic body and other paraganglia
- (D44.8) Pluriglandular involvement
  - Multiple endocrine adenomatosis
- (D 44.9) Endocrine gland, unspecified

(D 45.) Polycythaemia vera
(D 46.) Myelodysplastic syndromes
(D47.) Other neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue
- (D 47.0) Histiocytic and mast cell tumours of uncertain and unknown behaviour
- (D47.1) Chronic myeloproliferative disease
  - Myelofibrosis (with myeloid metaplasia)
  - Myeloproliferative disease, unspecified
  - Myelosclerosis (megakaryocytic) with myeloid metaplasia

- (D 47.2) Monoclonal gammopathy
- (D 47.3) Essential (haemorrhagic) thrombocythaemia
- (D 47.7) Other specified neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue
- (D 47.9) Neoplasm of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue, unspecified

(D 48.) Neoplasm of uncertain or unknown behaviour of other and unspecified sites

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

[edit] (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
(D 52.) Folate deficiency anaemia
(D 53.) Other nutritional anaemias

[edit] (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
- (D 58.0) Hereditary spherocytosis
- (D 58.1) Hereditary elliptocytosis
- (D 58.2) 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

[edit] (D60-D64) Aplastic and other anaemias

(D 60.) Acquired pure red cell aplasia (erythroblastopenia)
(D61.) Other aplastic anaemias
- (D61.0) Constitutional aplastic anaemia
  - Fanconi anemia
(D 62.) Acute posthaemorrhagic anaemia
(D 63.) Anaemia in chronic diseases classified elsewhere
(D 64.) Other anaemias

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

(D 65.) Disseminated intravascular coagulation (defibrination syndrome)

(D66.) Hereditary factor VIII deficiency
- Haemophilia A

(D67.) Hereditary factor IX deficiency
- Christmas disease

(D68.) Other coagulation defects
- (D 68.0) Von Willebrand's disease
- (D68.1) Hereditary factor XI deficiency
  - Haemophilia C
- (D 68.2) Hereditary deficiency of other clotting factors
- (D 68.3) Haemorrhagic disorder due to circulating anticoagulants
- (D 68.4) Acquired coagulation factor deficiency
- (D 68.8) Other specified coagulation defects
- (D 68.9) Coagulation defect, unspecified

(D69.) Purpura and other haemorrhagic conditions
- (D 69.0) Allergic purpura
- (D69.1) Qualitative platelet defects
  - Bernard-Soulier syndrome (giant platelet)
  - Glanzmann's disease
  - Grey platelet syndrome
  - Thromboasthenia (haemorrhagic)(hereditary)
  - Thrombocytopathy
- (D 69.2) Other nonthrombocytopenic purpura
- (D 69.3) Idiopathic thrombocytopenic purpura
- (D 69.4) Other primary thrombocytopenia
- (D 69.5) Secondary thrombocytopenia
- (D 69.6) Thrombocytopenia, unspecified
- (D 69.8) Other specified haemorrhagic conditions
- (D 69.9) Haemorrhagic condition, unspecified

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

(D70.) Agranulocytosis
- Neutropenia
(D 71.) Functional disorders of polymorphonuclear neutrophils

(D72.) Other disorders of white blood cells
- (D 72.1) Eosinophilia
- (D72.8) Other specified disorders of white blood cells
  - Leukocytosis
  - Lymphocytosis (symptomatic)
  - Lymphopenia
  - Monocytosis (symptomatic)
  - Plasmacytosis

(D 73.) Diseases of spleen
(D 74.) Methaemoglobinaemia

(D75.) Other diseases of blood and blood-forming organs
- (D 75.0) Familial erythrocytosis
- (D 75.1) Secondary polycythaemia
- (D 75.2) Essential thrombocytosis
- (D75.8) Other specified diseases of blood and blood-forming organs
  - Basophilia
- (D 75.9) Disease of blood and blood-forming organs, unspecified

(D76.) Certain diseases involving lymphoreticular tissue and reticulohistiocytic system
- (D76.0) Langerhans' cell histiocytosis, not elsewhere classified
- (D 76.1) Haemophagocytic lymphohistiocytosis
- (D 76.2) Haemophagocytic syndrome, infection-associated
- (D 76.3) Other histiocytosis syndromes

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

[edit] (D80-D89) Certain disorders involving the immune mechanism

(D80.) Immunodeficiency with predominantly antibody defects
- (D 80.0) Hereditary hypogammaglobulinaemia
- (D 80.1) 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
(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 (ADA) deficiency
- (D 81.4) Nezelof's syndrome
- (D 81.5) Purine nucleoside phosphorylase (PNP) deficiency
- (D 81.6) Major histocompatibility complex class I deficiency
- (D 81.7) Major histocompatibility complex class II deficiency
(D82.) Immunodeficiency associated with other major defects
- (D 82.0) Wiskott-Aldrich syndrome
- (D 82.1) Di George's syndrome
- (D 82.2) Immunodeficiency with short-limbed stature
- (D 82.3) Immunodeficiency following hereditary defective response to Epstein-Barr virus
- (D 82.4) Hyperimmunoglobulin E (IgE) syndrome
(D 83.) Common variable immunodeficiency
(D 84.) Other immunodeficiencies
(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
- (D 89.0) Polyclonal hypergammaglobulinaemia
- (D 89.1) Cryoglobulinaemia

Category: Medical manuals

ICD-10 Chapter II: Neoplasms; Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism

From Wikipedia, the free encyclopedia

Contents

[edit] C00-D48 - Neoplasms

[edit] (C00-C14) Malignant neoplasms, lip, oral cavity and pharynx

[edit] (C15-C26) Malignant neoplasms, digestive organs

[edit] (C30-C39) Malignant neoplasms, respiratory system and intrathoracic organs

[edit] (C40-C41) Malignant neoplasms, bone and articular cartilage

[edit] (C43-C44) Malignant neoplasms, skin

[edit] (C45-C49) Malignant neoplasms, connective and soft tissue

[edit] (C50-C58) Malignant neoplasms, breast and female genital organs

[edit] (C60-C63) Malignant neoplasms, male genital organs

[edit] (C64-C68) Malignant neoplasms, urinary organs

[edit] (C69-C72) Malignant neoplasms, nervous system

[edit] (C73-C75) Malignant neoplasms, endocrine glands and related structures

[edit] (C76-C80) Malignant neoplasms, secondary and ill-defined

[edit] (C81-C96) Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue

[edit] (C97) Malignant neoplasms of independent (primary) multiple sites

[edit] (D00-D09) In situ neoplasms

[edit] (D10-D36) Benign neoplasms

[edit] (D37-D48) Neoplasms of uncertain or unknown behaviour

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

[edit] (D50-D53) Nutritional anemias

[edit] (D55-D59) Haemolytic anaemias

[edit] (D60-D64) Aplastic and other anaemias

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

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

[edit] (D80-D89) Certain disorders involving the immune mechanism

[edit] See also

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