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Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)
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[]
- (C17) Malignant neoplasms of small intestine
- (C18) Malignant neoplasm of colon
- (C19) Malignant neoplasm of rectosigmoid junction
- (C20) Malignant neoplasm of rectum
- (C21) Malignant neoplasms of anus and anal canal
- (C22) Malignant neoplasms of liver and intrahepatic bile ducts
- (C23) Malignant neoplasm of gallbladder
- (C24) Malignant neoplasm of other and unspecified parts of biliary tract
- (C25) Malignant neoplasm of pancreas
- (C26) Malignant neoplasms of other and ill-defined Digestive Organs
(C30-C39) Malignant neoplasms, respiratory system and intrathoracic organs[]
- (C30) Malignant neoplasm of nasal cavity and middle ear
- (C300) Nasal cavity
- (C301) Middle ear
- (C31) Malignant neoplasm of accessory sinuses
- (C32) Malignant neoplasm of larynx
- (C33) Malignant neoplasm of trachea
- (C34) Malignant neoplasm of bronchus and lung
- (C37) Malignant neoplasm of thymus
- (C38) Malignant neoplasm of heart, mediastinum and pleura
- (C39) Malignant neoplasms of other and ill-defined sites in 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[]
(C45-C49) Malignant neoplasms, connective and soft tissue[]
- (C45) Mesothelioma
- (C46) Kaposi's Sarcoma
- (C47) Malignant neoplasm of peripheral nerves and autonomic nervous system
- (C48) Malignant neoplasm of retroperitoneum and peritoneum
- (C480) Retroperitoneum
- (C481) Specified parts of peritoneum
- (C482) Peritoneum, unspecified
- (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[]
- (C50) Malignant neoplasm of breast
- (C51) Malignant neoplasm of vulva
- (C52) Malignant neoplasm of vagina
- (C53) Malignant neoplasm of cervix uteri
- (C55) Malignant neoplasm of uterus, part unspecified
- (C56) Malignant neoplasm of ovary
- (C57) Malignant neoplasms of other and unspecified female and genital organs
- (C58) Malignant neoplasm of placenta
- Choriocarcinoma NOS
- Chorionepithelioma NOS
(C60-C63) Malignant neoplasms, male genital organs[]
- (C60) Malignant neoplasm of penis
- (C61) Malignant neoplasm of prostate
- (C62) Malignant neoplasm of testis
- (C63) Malignant neoplasm of other and unspecified male genital organs
(C64-C68) Malignant neoplasms, urinary organs[]
- (C64) Malignant neoplasm of kidney, except renal pelvis
- Wilms' tumor
- (C65) Malignant neoplasm of renal pelvis
- (C66) Malignant neoplasm of ureter
- (C67) Malignant neoplasm of bladder
- (C68) Malignant neoplasm of other and unspecified urinary organs
(C69-C72) Malignant neoplasms, nervous system[]
- (C70) Malignant neoplasm of meninges
- (C700) Cerebral meninges
- (C701) Spinal meninges
- (C71) Malignant neoplasm of brain
- (C710) Cerebrum, except lobes and ventricles
- (C711) Frontal lobe
- (C712) Temporal lobe
- (C713) Parietal lobe
- (C714) Occipital lobe
- (C715) Cerebral ventricle
- (C716) Cerebellum
- (C717) Brain stem
- (C718) Overlapping lesion of brain
- (C719) Brain, unspecified
- (C72) Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system
- (C720) Spinal cord
- (C721) Cauda equina
- (C722) Olfactory nerve
- (C723) Optic nerve
- (C724) Acoustic nerve
- (C725) Other and unspecified cranial nerves
- (C728) Overlapping lesion of brain and other parts of central nervous system
- (C729) Central nervous system, unspecified
[]
- (C73) Malignant neoplasm of thyroid gland
- (C74) Malignant neoplasm of adrenal gland
- (C740) Cortex of adrenal gland
- (C741) Medulla of adrenal gland
- (C749) Adrenal gland, unspecified
- Neuroblastoma, NOS
- (C75) Malignant neoplasm of other endocrine glands and related structures
(C76-C80) Malignant neoplasms, secondary and ill-defined[]
- (C76) Malignant neoplasm of other and ill-defined sites
- (C77) Secondary and unspecified malignant neoplasm of lymph nodes
- (C78) Secondary malignant neoplasm of respiratory and digestive organs
- (C79) Secondary malignant neoplasm of other sites
- (C80) Malignant neoplasm without specification of site
[]
- (C81) Hodgkin's Disease
- (C82) Follicular non-Hodgkin's lymphoma (nodular)
- (C83) Diffuse non-Hodgkin's lymphoma
- (C84) Peripheral and cutaneous T-cell lymphomas
- (C85) Other and unspecified types of non-Hodgkin's lymphoma
- (C90) Multiple myeloma and malignant plasma cell neoplasms
- (C900) Multiple myeloma
- (C901) Plasma cell leukaemia
- (C902) Plasmacytoma, extramedullary
- (C91) Lymphoid leukaemia
- (C92) Myeloid leukaemia
- (C93) Monocytic leukaemia
- (C94) Other leukaemias of specified cell type
- (C95) Leukaemia of unspecified cell type
- (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[]
- (C97) Malignant neoplasms of independent (primary) multiple sites
(D00-D09) In situ neoplasms[]
- (D00) Carcinoma in situ of oral cavity, oesophagus and stomach
- (D01) Carcinoma in situ of other and unspecified digestive organs
- (D02) Carcinoma in situ of middle ear and respiratory system
- (D03) Melanoma in situ
- (D04) Carcinoma in situ of skin
- (D05) Carcinoma in situ of breast
- (D06) Carcinoma in situ of cervix uteri
- (D07) Carcinoma in situ of other and unspecified genital organs
- (D09) Carcinoma in situ of other and unspecified sites
(D10-D36) Benign neoplasms[]
- (D11) Benign neoplasm of major salivary glands
- Warthin's tumor
- Pleomorphic adenoma
- (D110) Parotid gland
- (D117) Other major salivary glands
- (D119) Major salivary gland, unspecified
- (D13) Benign neoplasm of other and ill-defined parts of digestive system
- (D130) Oesophagus
- (D131) Stomach
- (D132) Duodenum
- (D133) Other and unspecified parts of small intestine
- (D134) Liver
- Intrahepatic bile ducts
- (D135) Extrahepatic bile ducts
- (D136) 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
- (D140) Middle ear, nasal cavity and accessory sinuses
- (D141) Larynx
- (D142) Trachea
- (D143) Bronchus and lung
- (D144) Respiratory system, unspecified
- (D15) Benign neoplasm of other and unspecified intrathoracic organs
- (D16) Benign neoplasm of bone and articular cartilage
- (D160) Scapula and long bones of upper limb
- (D161) Short bones of upper limb
- (D162) Long bones of lower limb
- (D163) Short bones of lower limb
- (D164) Bones of skull and face
- (D165) Lower jaw bone
- (D166) Vertebral column
- (D167) Ribs, sternum and clavicle
- (D168) Pelvic bones, sacrum and coccyx
- (D169) 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
- (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
- (D23) Other benign neoplasms of skin
- (D26) Other benign neoplasms of uterus
- (D28) Benign neoplasm of other and unspecified female genital organs
- (D29) Benign neoplasm of male genital organs
- (D30) Benign neoplasm of urinary organs
- (D33) Benign neoplasm of brain and other parts of central nervous system
- (D34) Benign neoplasm of thyroid gland
- (D35) Benign neoplasm of other and unspecified endocrine glands
- (D350) Adrenal gland
- (D351) Parathyroid gland
- (D352) Pituitary gland
- (D353) Craniopharyngeal duct
- (D354) Pineal gland
- (D355) Carotid body
- (D356) Aortic body and other paraganglia
- (D357) Other specified endocrine glands
- (D358) Pluriglandular involvement
- (D359) Endocrine gland, unspecified
- (D36) Benign neoplasm of other and unspecified sites
(D37-D48) Neoplasms of uncertain or unknown behaviour[]
- (D37) Neoplasm of uncertain or unknown behaviour of oral cavity and digestive organs
- (D38) 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
- (D40) Neoplasm of uncertain or unknown behaviour of male genital organs
- (D41) Neoplasm of uncertain or unknown behaviour of urinary organs
- (D42) Neoplasm of uncertain or unknown behaviour of meninges
- (D43) Neoplasm of uncertain or unknown behaviour of brain and central nervous system
- (D44) Neoplasm of uncertain or unknown behaviour of endocrine glands
- (D440) Thyroid gland
- (D441) Adrenal gland
- (D442) Parathyroid gland
- (D443) Pituitary gland
- (D444) Craniopharyngeal duct
- (D445) Pineal gland
- (D446) Carotid body
- (D447) Aortic body and other paraganglia
- (D448) Pluriglandular involvement
- Multiple endocrine adenomatosis
- (D449) Endocrine gland, unspecified
- (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
- (D470) Histiocytic and mast cell tumours of uncertain and unknown behaviour
- (D48) Neoplasm of uncertain or unknown behaviour of other and unspecified sites
- (D480) Bone and articular cartilage
- (D481) Connective and other soft tissue
- (D482) Peripheral nerves and autonomic nervous system
- (D483) Retroperitoneum
- (D484) Peritoneum
- (D485) Skin
- (D486) Breast
- (D487) Other specified sites
- (D489) Neoplasm of uncertain or unknown behaviour, 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
- (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
- (D510) Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
- (D53) Other nutritional anaemias
(D55-D59) Haemolytic anaemias[]
- (D55) Anaemia due to enzyme disorders
- (D550) Anaemia due to glucose-6-phosphate dehydrogenase (G6PD) deficiency
- Favism
- G6PD deficiency anaemia
- (D551) Anaemia due to other disorders of glutathione metabolism
- (D552) Anaemia due to disorders of glycolytic enzymes
- (D553) Anaemia due to disorders of nucleotide metabolism
- (D558) Other anaemias due to enzyme disorders
- (D559) Anaemia due to enzyme disorder, unspecified
- (D550) Anaemia due to glucose-6-phosphate dehydrogenase (G6PD) deficiency
- (D56) Thalassaemia
- (D57) 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
- (D610) Constitutional aplastic anaemia
- (D62) Acute posthaemorrhagic anaemia
- (D63) Anaemia in chronic diseases classified elsewhere
- (D64) Other anaemias
(D65-D69) Coagulation defects, purpura and other haemorrhagic conditions[]
- (D65) Disseminated intravascular coagulation (defibrination syndrome)
- (D66) Hereditary factor VIII deficiency
- Haemophilia A
- (D67) Hereditary factor IX deficiency
- Christmas disease
- (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
- (D690) Allergic purpura
(D70-D77) Other diseases of blood and blood-forming organs[]
- (D70) Agranulocytosis
- Neutropenia
- (D71) Functional disorders of polymorphonuclear neutrophils
- (D72) Other disorders of white blood cells
- (D721) Eosinophilia
- (D728) Other specified disorders of white blood cells
- Leukocytosis
- Lymphocytosis (symptomatic)
- Lymphopenia
- Monocytosis (symptomatic)
- Plasmacytosis
- (D74) Methaemoglobinaemia
- (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
- (D760) Langerhans' cell histiocytosis, not elsewhere classified
(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
- (D800) Hereditary hypogammaglobulinaemia
- (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)
- (D820) Wiskott-Aldrich syndrome
- (D83) Common variable immunodeficiency
- (D84) Other immunodeficiencies
- (D840) Lymphocyte function antigen-1 (LFA-1) defect
- (D841) Defects in the complement system
- C1 esterase inhibitor deficiency (C1-INH)
- (D848) Other specified immunodeficiencies
- (D849) Immunodeficiency, unspecified
- (D86) Sarcoidosis
- (D860) Sarcoidosis of lung
- (D861) Sarcoidosis of lymph nodes
- (D862) Sarcoidosis of lung with sarcoidosis of lymph nodes
- (D863) Sarcoidosis of skin
- (D868) 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
- (D891) Cryoglobulinaemia
- (D892) Hypergammaglobulinaemia, unspecified
- (D898) Other specified disorders involving the immune mechanism, not elsewhere classified
- (D899) Disorder involving the immune mechanism, unspecified
- (D890) Polyclonal hypergammaglobulinaemia
See also[]
- List of ICD-10 codes
- International Statistical Classification of Diseases and Related Health Problems
- List of ICD-9 codes 140-239: Neoplasms
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 |
Pathology: hematology (primarily C81-C96/200-208, D45-D47, D50-D77/280-289) | |
|---|---|
| WBCs |
hematological malignancy (Lymphoma, leukemia) |
| RBCs/anemia/ hemoglobinopathy |
nutritional anemia: Iron deficiency anemia, Plummer-Vinson syndrome, Megaloblastic anemia (Pernicious anemia) |
| Coagulation/platelets |
coagulopathy: DIC • Hemophilia (A, B, C, XIII) • Von Willebrand disease |
| 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 |
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 | |
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