Wikia

(C95) Leukaemia of unspecified cell type
- (C 950) Acute leukaemia of unspecified cell type
- (C 951) Chronic leukaemia of unspecified cell type
- (C 952) Subacute leukaemia of unspecified cell type
- (C 957) Other leukaemia of unspecified cell type
- (C 959) Leukaemia, unspecified

(C96) Other and unspecified malignant neoplasms of lymphoid, haematopoietic and related tissue
- (C 960) Letterer-Siwe disease
- (C 961) Malignant histiocytosis
- (C962) Malignant mast cell tumour
  - Malignant mastocytosis
- (C 963) True histiocytic lymphoma
- (C 967) Other specified malignant neoplasms of lymphoid, haematopoietic and related tissue
- (C 969) Malignant neoplasm of lymphoid, haematopoietic and related tissue, unspecified

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

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

(D00-D09) In situ neoplasms Edit

(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

(D10-D36) Benign neoplasms Edit

(D 10) Benign neoplasm of mouth and pharynx

(D11) Benign neoplasm of major salivary glands
- Warthin's tumor
- Pleomorphic adenoma
- (D 110) Parotid gland
- (D117) Other major salivary glands
  - Sublingual gland
  - Submandibular gland
- (D 119) Major salivary gland, unspecified

(D12) Benign neoplasm of colon, rectum, anus and anal canal
- Familial adenomatous polyposis
- (D 120) Caecum
- (D 121) Appendix
- (D 122) Ascending colon
- (D 123) Transverse colon
- (D 124) Descending colon
- (D 125) Sigmoid colon
- (D126) Colon, unspecified
  - Adenomatosis of colon
- (D 127) Rectosigmoid junction
- (D 128) Rectum
- (D 129) Anus and anal canal

(D13) Benign neoplasm of other and ill-defined parts of digestive system
- (D 130) Oesophagus
- (D 131) Stomach
- (D 132) Duodenum
- (D 133) Other and unspecified parts of small intestine
- (D134) Liver
  - Intrahepatic bile ducts
- (D 135) Extrahepatic bile ducts
- (D 136) Pancreas
- (D137) Endocrine pancreas
  - Islet cell tumour
  - Islets of Langerhans
- (D139) Ill-defined sites within the digestive system
  - Digestive system NOS
  - Intestine NOS
  - Spleen

(D14) Benign neoplasm of middle ear and respiratory system
- (D 140) Middle ear, nasal cavity and accessory sinuses
- (D 141) Larynx
- (D 142) Trachea
- (D 143) Bronchus and lung
- (D 144) Respiratory system, unspecified

(D15) Benign neoplasm of other and unspecified intrathoracic organs
- (D 150) Thymus
- (D151) Heart
  - Myxoma
- (D 152) Mediastinum

(D16) Benign neoplasm of bone and articular cartilage
- (D 160) Scapula and long bones of upper limb
- (D 161) Short bones of upper limb
- (D 162) Long bones of lower limb
- (D 163) Short bones of lower limb
- (D 164) Bones of skull and face
- (D 165) Lower jaw bone
- (D 166) Vertebral column
- (D 167) Ribs, sternum and clavicle
- (D 168) Pelvic bones, sacrum and coccyx
- (D 169) Bone and articular cartilage, unspecified

(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)

(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

(D30) Benign neoplasm of urinary organs
- (D 300) Kidney
- (D 301) [[Renal pelvis]
- (D 302) Ureter
- (D 303) Urinary bladder
- (D 304) Urethra
- (D 307) Other urinary organs
- (D 309) Urinary organ, unspecified

(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 350) Adrenal gland
- (D 351) Parathyroid gland
- (D352) Pituitary gland
  - Pituitary adenoma
  - Prolactinoma
- (D 353) Craniopharyngeal duct
- (D 354) Pineal gland
- (D 355) Carotid body
- (D 356) Aortic body and other paraganglia
- (D 357) Other specified endocrine glands
- (D 358) Pluriglandular involvement
- (D 359) Endocrine gland, unspecified

(D 36) Benign neoplasm of other and unspecified sites

(D37-D48) Neoplasms of uncertain or unknown behaviour Edit

(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
(D39) Neoplasm of uncertain or unknown behaviour of female genital organs
- (D 390) Uterus
- (D 391) Ovary
- (D 392) Placenta
- (D 397) Other female genital organs
- (D 399) Female genital organ, unspecified
(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 440) Thyroid gland
- (D 441) Adrenal gland
- (D 442) Parathyroid gland
- (D 443) Pituitary gland
- (D 444) Craniopharyngeal duct
- (D 445) Pineal gland
- (D 446) Carotid body
- (D 447) Aortic body and other paraganglia
- (D448) Pluriglandular involvement
  - Multiple endocrine adenomatosis
- (D 449) 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
- (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
- (D 472) Monoclonal gammopathy
- (D 473) Essential (haemorrhagic) thrombocythaemia
- (D 477) Other specified neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue
- (D 479) Neoplasm of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue, unspecified

(D48) Neoplasm of uncertain or unknown behaviour of other and unspecified sites
- (D 480) Bone and articular cartilage
- (D 481) Connective and other soft tissue
- (D 482) Peripheral nerves and autonomic nervous system
- (D 483) Retroperitoneum
- (D 484) Peritoneum
- (D 485) Skin
- (D 486) Breast
- (D 487) Other specified sites
- (D 489) Neoplasm of uncertain or unknown behaviour, unspecified

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

(D50-D53) Nutritional anemias Edit

(D50) Iron deficiency anaemia
- (D 500) Iron deficiency anaemia secondary to blood loss (chronic)
- (D501) Sideropenic dysphagia
  - Kelly-Paterson syndrome
  - Plummer-Vinson syndrome
- (D 508) Other iron deficiency anaemias
- (D 509) 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
- (D 512) Transcobalamin II deficiency
- (D 513) Other dietary vitamin B 12 deficiency anaemia
- (D 518) Other vitamin B 12 deficiency anaemias
- (D 519) Vitamin B 12 deficiency anaemia, unspecified

(D52) Folate deficiency anaemia
- (D520) Dietary folate deficiency anaemia
  - Nutritional megaloblastic anaemia
- (D 521) Drug-induced folate deficiency anaemia
- (D 528) Other folate deficiency anaemias
- (D 529) Folate deficiency anaemia, unspecified

(D53) Other nutritional anaemias
- (D 530) Protein deficiency anaemia
- (D 531) Other megaloblastic anaemias, not elsewhere classified
- (D 532) Scorbutic anaemia
- (D 538) Other specified nutritional anaemias
- (D 539) Nutritional anaemia, unspecified

(D55-D59) Haemolytic anaemias Edit

(D55) Anaemia due to enzyme disorders
- (D550) Anaemia due to glucose-6-phosphate dehydrogenase (G6PD) deficiency
  - Favism
  - G6PD deficiency anaemia
- (D 551) Anaemia due to other disorders of glutathione metabolism
- (D 552) Anaemia due to disorders of glycolytic enzymes
- (D 553) Anaemia due to disorders of nucleotide metabolism
- (D 558) Other anaemias due to enzyme disorders
- (D 559) Anaemia due to enzyme disorder, unspecified

(D56) Thalassaemia
- (D 560) Alpha thalassaemia
- (D 561) Beta thalassaemia
- (D 562) Delta-beta thalassaemia
- (D 563) Thalassaemia trait
- (D 564) Hereditary persistence of fetal haemoglobin (HPFH)
- (D 568) Other thalassaemias
- (D 569) Thalassaemia, unspecified

(D57) Sickle-cell disorders
- (D 570) Sickle-cell anaemia with crisis
- (D 571) Sickle-cell anaemia without crisis
- (D 572) Double heterozygous sickling disorders
- (D 573) Sickle-cell trait
- (D 578) Other sickle-cell disorders

(D58) Other hereditary haemolytic anaemias
- (D 580) Hereditary spherocytosis
- (D 581) Hereditary elliptocytosis
- (D 582) Other haemoglobinopathies
- (D588) Other specified hereditary haemolytic anaemias
  - Stomatocytosis

(D59) Acquired haemolytic anaemia
- (D 590) Drug-induced autoimmune haemolytic anaemia
- (D591) Other autoimmune haemolytic anaemias
  - Warm autoimmune hemolytic anemia
- (D 592) Drug-induced nonautoimmune haemolytic anaemia
- (D 593) Haemolytic-uraemic syndrome
- (D594) Other nonautoimmune haemolytic anaemias
  - Microangiopathic hemolytic anemia
- (D 595) Paroxysmal nocturnal haemoglobinuria (Marchiafava-Micheli)
- (D596) Haemoglobinuria due to haemolysis from other external causes
  - paroxysmal cold haemoglobinuria
- (D 598) Other acquired haemolytic anaemias
- (D 599) Acquired haemolytic anaemia, unspecified

(D60-D64) Aplastic and other anaemias Edit

(D 60) Acquired pure red cell aplasia (erythroblastopenia)
(D61) Other aplastic anaemias
- (D610) Constitutional aplastic anaemia
  - Fanconi anemia
(D 62) Acute posthaemorrhagic anaemia
(D 63) Anaemia in chronic diseases classified elsewhere

(D64) Other anaemias
- (D 640) Hereditary sideroblastic anaemia
- (D 641) Secondary sideroblastic anaemia due to disease
- (D 642) Secondary sideroblastic anaemia due to drugs and toxins
- (D 643) Other sideroblastic anaemias
- (D 644) Congenital dyserythropoietic anaemia
- (D 648) Other specified anaemias
- (D 649) Anaemia, unspecified

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

(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 680) Von Willebrand's disease
- (D681) Hereditary factor XI deficiency
  - Haemophilia C
- (D 682) Hereditary deficiency of other clotting factors
- (D 683) Haemorrhagic disorder due to circulating anticoagulants
- (D 684) Acquired coagulation factor deficiency
- (D 688) Other specified coagulation defects
- (D 689) 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
- (D 692) Other nonthrombocytopenic purpura
- (D693) Idiopathic thrombocytopenic purpura
  - Evans' syndrome
- (D 694) Other primary thrombocytopenia
- (D 695) Secondary thrombocytopenia
- (D 696) Thrombocytopenia, unspecified
- (D 698) Other specified haemorrhagic conditions
- (D 699) Haemorrhagic condition, unspecified

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

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

(D72) Other disorders of white blood cells
- (D 721) Eosinophilia
- (D728) Other specified disorders of white blood cells
  - Leukocytosis
  - Lymphocytosis (symptomatic)
  - Lymphopenia
  - Monocytosis (symptomatic)
  - Plasmacytosis

(D73) Diseases of spleen
- (D 730) Hyposplenism
- (D 731) Hypersplenism
- (D 732) Chronic congestive splenomegaly
- (D 733) Abscess of spleen
- (D 734) Cyst of spleen
- (D 735) Infarction of spleen
- (D 738) Other diseases of spleen
- (D 739) Disease of spleen, unspecified

(D 74) Methaemoglobinaemia

(D75) Other diseases of blood and blood-forming organs
- (D 750) Familial erythrocytosis
- (D 751) Secondary polycythaemia
- (D 752) Essential thrombocytosis
- (D758) Other specified diseases of blood and blood-forming organs
  - Basophilia
- (D 759) Disease of blood and blood-forming organs, unspecified

(D76) Certain diseases involving lymphoreticular tissue and reticulohistiocytic system
- (D760) Langerhans' cell histiocytosis, not elsewhere classified
- (D761) Haemophagocytic lymphohistiocytosis
  - Familial haemophagocytic reticulosis
- (D 762) Haemophagocytic syndrome, infection-associated
- (D763) Other histiocytosis syndromes
  - Reticulohistiocytoma (giant-cell)
  - Sinus histiocytosis with massive lymphadenopathy
  - Xanthogranuloma

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

(D80-D89) Certain disorders involving the immune mechanism Edit

(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
- (D 802) Selective deficiency of immunoglobulin A (IgA)
- (D 803) Selective deficiency of immunoglobulin G (IgG) subclasses
- (D 804) Selective deficiency of immunoglobulin M (IgM)
- (D 805) Immunodeficiency with increased immunoglobulin M (IgM)
- (D 806) Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
- (D 807) Transient hypogammaglobulinaemia of infancy
- (D808) Other immunodeficiencies with predominantly antibody defects
  - Kappa light chain deficiency
- (D 808) Immunodeficiency with predominantly antibody defects, unspecified

(D81) Combined immunodeficiencies
- (D 810) Severe combined immunodeficiency (SCID) with reticular dysgenesis
- (D 811) Severe combined immunodeficiency (SCID) with low T-cell and B-cell numbers
- (D 812) Severe combined immunodeficiency (SCID) with low or normal B-cell numbers
- (D 813) Adenosine deaminase deficiency (ADA)
- (D 814) Nezelof's syndrome
- (D 815) Purine nucleoside phosphorylase deficiency (PNP)
- (D816) Major histocompatibility complex class I deficiency
  - Bare lymphocyte syndrome
- (D 817) 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
- (D 821) Di George's syndrome
- (D 822) Immunodeficiency with short-limbed stature
- (D823) Immunodeficiency following hereditary defective response to Epstein-Barr virus
  - X-linked lymphoproliferative disease
- (D 824) Hyperimmunoglobulin E syndrome (IgE)
(D 83) Common variable immunodeficiency

(D84) Other immunodeficiencies
- (D 840) Lymphocyte function antigen-1 (LFA-1) defect
- (D841) Defects in the complement system
  - C1 esterase inhibitor deficiency (C1-INH)
- (D 848) Other specified immunodeficiencies
- (D 849) Immunodeficiency, unspecified

(D86) Sarcoidosis
- (D 860) Sarcoidosis of lung
- (D 861) Sarcoidosis of lymph nodes
- (D 862) Sarcoidosis of lung with sarcoidosis of lymph nodes
- (D 863) Sarcoidosis of skin
- (D 868) Sarcoidosis of other and combined sites
(D89) Other disorders involving the immune mechanism, not elsewhere classified
- (D890) Polyclonal hypergammaglobulinaemia
  - Benign hypergammaglobulinaemic purpura
  - Polyclonal gammopathy NOS
- (D 891) Cryoglobulinaemia
- (D 892) Hypergammaglobulinaemia, unspecified
- (D 898) Other specified disorders involving the immune mechanism, not elsewhere classified
- (D 899) Disorder involving the immune mechanism, unspecified

v·d·e Pathology: Tumors, neoplasia, and oncology (C00-D48, 140-239)
Benign tumors	Hyperplasia - Cyst - Pseudocyst - Hamartoma - Benign neoplasm
Malignant progression	Dysplasia - Carcinoma in situ - Invasive cancer - Metastasis
Topography	Anus - Bladder - Blood - Bile duct - Bone - Brain - Breast - Cervix - Colon/rectum - Endometrium - Esophagus - Eye - Gallbladder - Head/Neck - Liver - Kidney - Larynx - Lung - Mediastinum (chest) - Mouth - Ovaries - Pancreas - Penis - Prostate - Skin - Small intestine - Stomach - Tailbone - Testicles - Thyroid
Misc.	Tumor suppressor genes/oncogenes - Staging/grading - Carcinogenesis - Carcinogen - Research - Paraneoplastic syndrome - List of oncology-related terms

v·d·e Pathology: hematology (primarily C81-C96/200-208, D45-D47, D50-D77/280-289)
WBCs	hematological malignancy (Lymphoma, leukemia) -cytosis (Agranulocytosis, Leukocytosis, Lymphocytosis, Monocytosis) • -penia (Lymphopenia, Neutropenia)
RBCs/anemia/ hemoglobinopathy	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: Warm autoimmune hemolytic anemia, HUS, MAHA, PNH aplastic anemia: Acquired PRCA, Diamond-Blackfan anemia, Fanconi anemia • Sideroblastic anemia • Hemochromatosis
Coagulation/platelets	coagulopathy: DIC • Hemophilia (A, B, C, XIII) • Von Willebrand disease Purpura: Henoch-Schönlein, ITP, TTP primary hypercoagulable state: Protein C deficiency - Protein S deficiency - Antithrombin III deficiency other hemorrhagic conditions: Bernard-Soulier syndrome - Glanzmann's thrombasthenia - Grey platelet syndrome
Histiocytosis	WHO-I Langerhans cell histiocytosis - non-Langerhans-cell histiocytosis/WHO-II (Juvenile xanthogranuloma, Hemophagocytic lymphohistiocytosis) - malignant histiocytic disorders/WHO-III (Acute monocytic leukemia, Malignant histiocytosis, Erdheim-Chester disease)
Other	Asplenia/hyposplenism - Methemoglobinemia

v·d·e Pathology: Immune disorders (primarily D80-D89, 273, 279)
Antibody defects	X-linked agammaglobulinemia - Selective immunoglobulin A deficiency
Combined immunodeficiencies	Severe combined immunodeficiency (X-SCID) - Adenosine deaminase deficiency - Nezelof syndrome - Purine nucleoside phosphorylase deficiency - Bare lymphocyte syndrome
Other	Wiskott-Aldrich syndrome - DiGeorge syndrome - Hyper-IgE syndrome - Common variable immunodeficiency - Complement deficiency (Angioedema) - Sarcoidosis - Hypergammaglobulinemia - Cryoglobulinemia - Paraproteinemia - Immunodeficiency/Primary immunodeficiency
Autoimmunity	see list of autoimmune diseases

Wikia

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

Contents

C00-D48 - NeoplasmsEdit

(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 mechanismEdit

(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 alsoEdit

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