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Contents

C00-D48 - Neoplasms

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

  • (C00) Malignant neoplasm of lip
  • (C01) Malignant neoplasm of base of tongue
  • (C02) Malignant neoplasm of other and unspecified parts of tongue
  • (C03) Malignant neoplasm of gum
  • (C04) Malignant neoplasm of floor of mouth
  • (C05) Malignant neoplasm of palate
  • (C06) Malignant neoplasm of other and unspecified parts of mouth
  • (C07) Malignant neoplasm of parotid gland
  • (C08) Malignant neoplasm of other and unspecified major salivary glands
  • (C09) Malignant neoplasm of tonsil
  • (C10) Malignant neoplasm of oropharynx
  • (C11) Malignant neoplasm of nasopharynx
  • (C12) Malignant neoplasm of piriform sinus
  • (C13) Malignant neoplasm of hypopharynx
  • (C14) Malignant neoplasm of other and ill-defined sites in the lip, oral cavity and pharynx

(C15-C26) Malignant neoplasms, digestive organs

  • (C15) Malignant neoplasm of Esophagus
  • (C16) Malignant neoplasm of Stomach
    • (C160) Cardia
    • (C161) Fundus of stomach
    • (C162) Body of stomach
    • (C163) Pyloric antrum
    • (C164) Pylorus
    • (C165) Lesser curvature of stomach, unspecified
    • (C166) Greater curvature of stomach, unspecified
    • (C168) Overlapping lesion of stomach
    • (C169) Stomach, unspecified
  • (C18) Malignant neoplasm of colon
    • (C180) Caecum
    • (C181) Appendix
    • (C182) Ascending colon
    • (C183) Hepatic flexure
    • (C184) Transverse colon
    • (C185) Splenic flexure
    • (C186) Descending colon
    • (C187) Sigmoid colon
    • (C188) Overlapping lesion of colon
    • (C189) Colon, unspecified
  • (C19) Malignant neoplasm of rectosigmoid junction
  • (C20) Malignant neoplasm of rectum
  • (C21) Malignant neoplasms of anus and anal canal
  • (C23) Malignant neoplasm of gallbladder
  • (C24) Malignant neoplasm of other and unspecified parts of biliary tract
  • (C25) Malignant neoplasm of pancreas

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

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

  • (C40) Malignant neoplasm of bone and articular cartilage of limbs
  • (C41) Malignant neoplasm of bone and articular cartilage of other and unspecified sites

(C43-C44) Malignant neoplasms, skin

  • (C43) Malignant melanoma of Skin
  • (C44) Other malignant neoplasms of skin

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

  • (C49) Malignant neoplasm of other connective and soft tissue
    • C49.M10 Malignant fibrous histiocytoma
    • C49.M12 Atypical fibroxanthoma
    • C49.M20 Haemangiopericytoma
    • C49.M22 Angioendotheliomatosis, malignant
    • C49.M24 Dermatofibrosarcoma protruberans
    • C49.M30 Bednar tumour
    • C49.M40 Sarcoma of skin
    • C49.M42 Fibrosarcoma
    • C49.M44 Schwannoma, malignant
    • C49.M48 Leiomyosarcoma
    • C49.M50 Rhabdomyosarcoma
    • C49.M54 Myxofibrosarcoma
    • C49.M60 Angiosarcoma, cutaneous
    • C49.M70 Lymphangiosarcoma

(Alphanumeric subcodes are ILDS.)

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

  • (C54) Malignant neoplasm of corpus uteri
    • (C541) Endometrial cancer

(C60-C63) Malignant neoplasms, male genital organs

(C64-C68) Malignant neoplasms, urinary organs

(C69-C72) Malignant neoplasms, nervous system

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

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

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

  • (C81) Hodgkin's Disease
    • (C810) Lymphocytic predominance
    • (C811) Nodular sclerosis
    • (C812) Mixed cellularity
    • (C813) Lymphocytic depletion
  • (C82) Follicular non-Hodgkin's lymphoma (nodular)
    • (C820) Small cleaved cell, follicular
    • (C821) Mixed small cleaved and large cell, follicular
    • (C822) Large cell, follicular
  • (C83) Diffuse non-Hodgkin's lymphoma
    • (C830) Small cell (diffuse)
    • (C831) Small cleaved cell (diffuse)
    • (C832) Mixed small and large cell (diffuse)
    • (C833) Large cell (diffuse)
    • (C834) Immunoblastic (diffuse)
    • (C835) Lymphoblastic (diffuse)
    • (C836) Undifferentiated (diffuse)
    • (C837) Burkitt's tumour
  • (C84) Peripheral and cutaneous T-cell lymphomas
    • (C840) Mycosis fungoides
    • (C841) Sézary's disease
    • (C842) T-zone lymphoma
    • (C843) Lymphoepithelioid lymphoma
    • (C844) Peripheral T-cell lymphoma
  • (C85) Other and unspecified types of non-Hodgkin's lymphoma
    • (C850) Lymphosarcoma
    • (C851) B-cell lymphoma, unspecified
  • (C88) Malignant immunoproliferative diseases
    • (C880) Waldenström's macroglobulinaemia
    • (C881) Alpha heavy chain disease
    • (C882) Gamma heavy chain disease
    • (C883) Immunoproliferative small intestinal disease
  • (C91) Lymphoid leukaemia
    • (C910) Acute lymphoblastic leukaemia
    • (C911) Chronic lymphocytic leukaemia
    • (C914) Hairy-cell leukaemia
  • (C92) Myeloid leukaemia
    • (C920) Acute myeloid leukaemia
    • (C921) Chronic myeloid leukaemia
    • (C922) Subacute myeloid leukaemia
    • (C923) Myeloid sarcoma
      • Chloroma
      • Granulocytic sarcoma
    • (C924) Acute promyelocytic leukaemia
    • (C925) Acute myelomonocytic leukaemia
  • (C93) Monocytic leukaemia
    • (C930) Acute monocytic leukaemia
    • (C931) Chronic monocytic leukaemia
    • (C932) Subacute monocytic leukaemia
  • (C94) Other leukaemias of specified cell type
    • (C940) Acute erythraemia and erythroleukaemia
      • Di Guglielmo's disease
    • (C941) Chronic erythraemia
    • (C942) Acute megakaryoblastic leukaemia
    • (C943) Mast cell leukaemia
    • (C944) Acute panmyelosis
    • (C945) Acute myelofibrosis
    • (C947) Other specified leukaemias
  • (C95) Leukaemia of unspecified cell type
    • (C950) Acute leukaemia of unspecified cell type
    • (C951) Chronic leukaemia of unspecified cell type
    • (C952) Subacute leukaemia of unspecified cell type
    • (C957) Other leukaemia of unspecified cell type
    • (C959) Leukaemia, unspecified
  • (C96) Other and unspecified malignant neoplasms of lymphoid, haematopoietic and related tissue
    • (C960) Letterer-Siwe disease
    • (C961) Malignant histiocytosis
    • (C962) Malignant mast cell tumour
      • Malignant mastocytosis
    • (C963) True histiocytic lymphoma
    • (C967) Other specified malignant neoplasms of lymphoid, haematopoietic and related tissue
    • (C969) Malignant neoplasm of lymphoid, haematopoietic and related tissue, unspecified

(C97) Malignant neoplasms of independent (primary) multiple sites

(D00-D09) In situ neoplasms

(D10-D36) Benign neoplasms

  • (D15) Benign neoplasm of other and unspecified intrathoracic organs
  • (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
    • (D180) Haemangioma, any site
      • Angioma NOS
    • (D181) Lymphangioma, any site
      • Cavernous haemangioma (ILDS D18.014)
  • (D19) Benign neoplasm of mesothelial tissue
  • (D20) 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)
  • (D22) Melanocytic naevi
  • (D25) Leiomyoma of uterus
    • Uterine fibroids
  • (D28) Benign neoplasm of other and unspecified female genital organs
  • (D29) Benign neoplasm of male genital organs
  • (D31) Benign neoplasm of eye and adnexa
  • (D36) Benign neoplasm of other and unspecified sites

(D37-D48) Neoplasms of uncertain or unknown behaviour

  • (D45) Polycythaemia vera
  • (D46) Myelodysplastic syndromes
  • (D47) Other neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue
    • (D470) Histiocytic and mast cell tumours of uncertain and unknown behaviour
      • Mast cell tumour NOS
      • Mastocytoma NOS
    • (D471) Chronic myeloproliferative disease
      • Myelofibrosis (with myeloid metaplasia)
      • Myeloproliferative disease, unspecified
      • Myelosclerosis (megakaryocytic) with myeloid metaplasia
    • (D472) Monoclonal gammopathy
    • (D473) Essential (haemorrhagic) thrombocythaemia
    • (D477) Other specified neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue
    • (D479) Neoplasm of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue, unspecified

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
    • (D500) Iron deficiency anaemia secondary to blood loss (chronic)
    • (D501) Sideropenic dysphagia
      • Kelly-Paterson syndrome
      • Plummer-Vinson syndrome
    • (D508) Other iron deficiency anaemias
    • (D509) Iron deficiency anaemia, unspecified
  • (D51) Vitamin B12 deficiency anaemia
    • (D510) Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
      • Pernicious anemia
    • (D511) Vitamin B 12 deficiency anaemia due to selective vitamin B 12 malabsorption with proteinuria
      • Megaloblastic hereditary anaemia
    • (D512) Transcobalamin II deficiency
    • (D513) Other dietary vitamin B 12 deficiency anaemia
    • (D518) Other vitamin B 12 deficiency anaemias
    • (D519) Vitamin B 12 deficiency anaemia, unspecified
  • (D52) Folate deficiency anaemia
    • (D520) Dietary folate deficiency anaemia
      • Nutritional megaloblastic anaemia
    • (D521) Drug-induced folate deficiency anaemia
    • (D528) Other folate deficiency anaemias
    • (D529) Folate deficiency anaemia, unspecified
  • (D53) Other nutritional anaemias
    • (D530) Protein deficiency anaemia
    • (D531) Other megaloblastic anaemias, not elsewhere classified
    • (D532) Scorbutic anaemia
    • (D538) Other specified nutritional anaemias
    • (D539) Nutritional anaemia, unspecified

(D55-D59) Haemolytic anaemias

  • (D56) Thalassaemia
    • (D560) Alpha thalassaemia
    • (D561) Beta thalassaemia
    • (D562) Delta-beta thalassaemia
    • (D563) Thalassaemia trait
    • (D564) Hereditary persistence of fetal haemoglobin (HPFH)
    • (D568) Other thalassaemias
    • (D569) Thalassaemia, unspecified
  • (D57) Sickle-cell disorders
    • (D570) Sickle-cell anaemia with crisis
    • (D571) Sickle-cell anaemia without crisis
    • (D572) Double heterozygous sickling disorders
    • (D573) Sickle-cell trait
    • (D578) Other sickle-cell disorders
  • (D58) Other hereditary haemolytic anaemias
    • (D580) Hereditary spherocytosis
    • (D581) Hereditary elliptocytosis
    • (D582) Other haemoglobinopathies
    • (D588) Other specified hereditary haemolytic anaemias
      • Stomatocytosis
  • (D59) Acquired haemolytic anaemia
    • (D590) Drug-induced autoimmune haemolytic anaemia
    • (D591) Other autoimmune haemolytic anaemias
      • Warm autoimmune hemolytic anemia
    • (D592) Drug-induced nonautoimmune haemolytic anaemia
    • (D593) Haemolytic-uraemic syndrome
    • (D594) Other nonautoimmune haemolytic anaemias
      • Microangiopathic hemolytic anemia
    • (D595) Paroxysmal nocturnal haemoglobinuria (Marchiafava-Micheli)
    • (D596) Haemoglobinuria due to haemolysis from other external causes
      • paroxysmal cold haemoglobinuria
    • (D598) Other acquired haemolytic anaemias
    • (D599) Acquired haemolytic anaemia, unspecified

(D60-D64) Aplastic and other anaemias

  • (D60) Acquired pure red cell aplasia (erythroblastopenia)
  • (D61) Other aplastic anaemias
    • (D610) Constitutional aplastic anaemia
      • Fanconi anemia
  • (D62) Acute posthaemorrhagic anaemia
  • (D63) Anaemia in chronic diseases classified elsewhere
  • (D64) Other anaemias
    • (D640) Hereditary sideroblastic anaemia
    • (D641) Secondary sideroblastic anaemia due to disease
    • (D642) Secondary sideroblastic anaemia due to drugs and toxins
    • (D643) Other sideroblastic anaemias
    • (D644) Congenital dyserythropoietic anaemia
    • (D648) Other specified anaemias
    • (D649) Anaemia, unspecified

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

  • (D65) Disseminated intravascular coagulation (defibrination syndrome)
  • (D68) Other coagulation defects
    • (D680) Von Willebrand's disease
    • (D681) Hereditary factor XI deficiency
      • Haemophilia C
    • (D682) Hereditary deficiency of other clotting factors
    • (D683) Haemorrhagic disorder due to circulating anticoagulants
    • (D684) Acquired coagulation factor deficiency
    • (D688) Other specified coagulation defects
    • (D689) Coagulation defect, unspecified
  • (D69) Purpura and other haemorrhagic conditions
    • (D690) Allergic purpura
      • anaphylactoid purpura
      • Henoch-Schönlein purpura
    • (D691) Qualitative platelet defects
      • Bernard-Soulier syndrome (giant platelet)
      • Glanzmann's disease
      • Grey platelet syndrome
      • Thromboasthenia (haemorrhagic)(hereditary)
      • Thrombocytopathy
    • (D692) Other nonthrombocytopenic purpura
    • (D693) Idiopathic thrombocytopenic purpura
      • Evans' syndrome
    • (D694) Other primary thrombocytopenia
    • (D695) Secondary thrombocytopenia
    • (D696) Thrombocytopenia, unspecified
    • (D698) Other specified haemorrhagic conditions
    • (D699) Haemorrhagic condition, unspecified

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

  • (D73) Diseases of spleen
    • (D730) Hyposplenism
    • (D731) Hypersplenism
    • (D732) Chronic congestive splenomegaly
    • (D733) Abscess of spleen
    • (D734) Cyst of spleen
    • (D735) Infarction of spleen
    • (D738) Other diseases of spleen
    • (D739) Disease of spleen, unspecified
  • (D74) Methaemoglobinaemia
  • (D75) Other diseases of blood and blood-forming organs
    • (D750) Familial erythrocytosis
    • (D751) Secondary polycythaemia
    • (D752) Essential thrombocytosis
    • (D758) Other specified diseases of blood and blood-forming organs
      • Basophilia
    • (D759) Disease of blood and blood-forming organs, unspecified
  • (D76) Certain diseases involving lymphoreticular tissue and reticulohistiocytic system
    • (D760) Langerhans' cell histiocytosis, not elsewhere classified
      • Eosinophilic granuloma
      • Hand-Schüller-Christian disease
      • Histiocytosis X (chronic)
    • (D761) Haemophagocytic lymphohistiocytosis
      • Familial haemophagocytic reticulosis
    • (D762) Haemophagocytic syndrome, infection-associated
    • (D763) Other histiocytosis syndromes
      • Reticulohistiocytoma (giant-cell)
      • Sinus histiocytosis with massive lymphadenopathy
      • Xanthogranuloma
  • (D77) 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
    • (D800) Hereditary hypogammaglobulinaemia
      • Autosomal recessive agammaglobulinaemia (Swiss type)
      • X-linked agammaglobulinaemia (Bruton) (with growth hormone deficiency)
    • (D801) Nonfamilial hypogammaglobulinaemia
      • Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes
      • Common variable agammaglobulinaemia (CVAgamma)
      • Hypogammaglobulinaemia NOS
    • (D802) Selective deficiency of immunoglobulin A (IgA)
    • (D803) Selective deficiency of immunoglobulin G (IgG) subclasses
    • (D804) Selective deficiency of immunoglobulin M (IgM)
    • (D805) Immunodeficiency with increased immunoglobulin M (IgM)
    • (D806) Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
    • (D807) Transient hypogammaglobulinaemia of infancy
    • (D808) Other immunodeficiencies with predominantly antibody defects
      • Kappa light chain deficiency
    • (D808) Immunodeficiency with predominantly antibody defects, unspecified
  • (D81) Combined immunodeficiencies
    • (D810) Severe combined immunodeficiency (SCID) with reticular dysgenesis
    • (D811) Severe combined immunodeficiency (SCID) with low T-cell and B-cell numbers
    • (D812) Severe combined immunodeficiency (SCID) with low or normal B-cell numbers
    • (D813) Adenosine deaminase deficiency (ADA)
    • (D814) Nezelof's syndrome
    • (D815) Purine nucleoside phosphorylase deficiency (PNP)
    • (D816) Major histocompatibility complex class I deficiency
      • Bare lymphocyte syndrome
    • (D817) Major histocompatibility complex class II deficiency
    • (D818) Other combined immunodeficiencies
      • Biotin-dependent carboxylase deficiency
    • (D819) Combined immunodeficiency, unspecified
      • Severe combined immunodeficiency disorder (SCID) NOS
  • (D82) Immunodeficiency associated with other major defects
    • (D820) Wiskott-Aldrich syndrome
      • Immunodeficiency with thrombocytopenia and eczema
    • (D821) Di George's syndrome
    • (D822) Immunodeficiency with short-limbed stature
    • (D823) Immunodeficiency following hereditary defective response to Epstein-Barr virus
      • X-linked lymphoproliferative disease
    • (D824) Hyperimmunoglobulin E syndrome (IgE)
  • (D83) Common variable immunodeficiency
  • (D84) Other immunodeficiencies
  • (D86) Sarcoidosis
  • (D89) Other disorders involving the immune mechanism, not elsewhere classified
    • (D890) Polyclonal hypergammaglobulinaemia
      • Benign hypergammaglobulinaemic purpura
      • Polyclonal gammopathy NOS
    • (D891) Cryoglobulinaemia
    • (D892) Hypergammaglobulinaemia, unspecified
    • (D898) Other specified disorders involving the immune mechanism, not elsewhere classified
    • (D899) Disorder involving the immune mechanism, unspecified

See also




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