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Attraction To Disability
Wikipedia
With time, the wish to become disabled is " projected " onto others. The analogy with Munchausen Syndrome (simulating or inducing illness as a route to compassion and benefits) here is reasonably clear in wannabes. ... See also [ edit ] Abasiophilia – the fascination for disabled people who use leg-braces or other orthopaedic appliances Agalmatophilia – the desire for mannequins or for statue-like immobility, feigned or caused by illness or paralysis Acrotomophilia – the desire for partners with missing limbs Apotemnophilia – the desire to acquire a disability ("wannabeism," "transability", "transabled"); Body integrity identity disorder BIID Body dysmorphic disorder – the pathological dislike of one's own physique for subjective reasons Body modification – the deliberate altering of physique for non-medical reasons Disability pretenders – one who behaves as if disabled and/or alters their appearance so as to suggest they are disabled Handicap fetishism – another term for the broad range of attractions to disability Handicap principle – possible analogue from the animal kingdom Legbrace fetishism – the desire for partners who use leg braces; an aspect of abasiophilia Medical fetishism – a sexualised interest in observing medical practice and receiving medical treatment Munchhausen's syndrome – a psychological disorder whose sufferers feign illness and/or cause themselves self-harm References [ edit ] ^ a b Limoncin, E.; Carta, R.; et al. (2014).
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Granuloma
Wikipedia
External links [ edit ] Classification D ICD - 10 : L92 ICD - 9-CM : 686.1 , 709.4 MeSH : D006099 SNOMED CT : 45647009 v t e Inflammation Symptoms Flushing (Rubor) Fever (Calor) Swelling (Tumor) Pain (Dolor) Malaise Mechanism Acute Plasma-derived mediators Bradykinin complement C3 C5a MAC coagulation Factor XII Plasmin Thrombin Cell-derived mediators preformed: Lysosome granules biogenic amines Histamine Serotonin synthesized on demand: cytokines IFN-γ IL-8 TNF-α IL-1 eicosanoids Leukotriene B4 Prostaglandins Nitric oxide Kinins Chronic Macrophage Epithelioid cell Giant cell Granuloma Other Acute-phase reaction Vasodilation Increased vascular permeability Exudate Leukocyte extravasation Chemotaxis Tests Full blood count Leukocytosis C-reactive protein Erythrocyte sedimentation rate General Lymphadenopathy List of inflammed body part states v t e Cutaneous keratosis, ulcer, atrophy, and necrobiosis Epidermal thickening keratoderma : Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis : Seborrheic keratosis Clonal seborrheic keratosis Common seborrheic keratosis Irritated seborrheic keratosis Seborrheic keratosis with squamous atypia Reticulated seborrheic keratosis Dermatosis papulosa nigra Keratosis punctata of the palmar creases other hyperkeratosis : Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Keloid Hypertrophic scar Cutis verticis gyrata Necrobiosis / granuloma Necrobiotic/palisading Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant-cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis / Interstitial granulomatous drug reaction Foreign body granuloma Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain Other/ungrouped eosinophilic dermatosis Granuloma faciale Dermis / localized CTD Cutaneous lupus erythematosus chronic: Discoid Panniculitis subacute : Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome Scleroderma / Morphea Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma Atrophic / atrophoderma Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin Perforating Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum / Pseudo-ainhum
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Open Fracture
Wikipedia
High index of suspicion of compartment syndrome should be maintained for leg and forearm fractures. [4] There are a number of classification systems attempting to categorise open fractures such as Gustilo open fracture classification , Tscherne classification , and Müller AO Classification of fractures . ... Both reamed and unreamed intramedullary nailing are accepted surgical treatments for open tibial fracture. [13] Both techniques have similar rates of postoperative healing, postoperative infection, implant failure and compartment syndrome. [13] Unreamed intramedullary nailing is advantageous because it has a lower incidence of superficial infection and malunion compared to external fixation . [14] However, unreamed intramedullary nailing can result in high rates of hardware failure if a person's weight bearing after surgery is not closely controlled. [14] Compared to external fixation, unreamed intramedullary nailing has similar rates of deep infection, delayed union and nonunion following surgery. [14] For open tibial fractures in children, there is an increasing trend of using orthopedic cast rather than external fixation.
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Loxoscelism
Wikipedia
Spider species blamed for necrosis in the past have included wolf spiders , white-tailed spiders , black house spiders , yellow sac spiders , orb weavers , and funnel-weaving spiders such as the hobo spider . [1] ^ Diseases that may cause symptoms similar to loxoscelism include: streptococcal or staphylococcal infection (particularly by methicillin -resistant Staphylococcus aureus ), herpes simplex, herpes zoster, diabetic ulcer, fungal infection, pyoderma gangrenosum, lymphomatoid papulosis, chemical burn, Toxicodendron dermatitis, squamous cell carcinoma, neoplasia, localized vasculitis, syphilis, Stevens-Johnson syndrome, toxic epidermal necrolysis, erythema nodosum, erythema multiforme, gonococcemia, purpura fulminans, sporotrichosis, Lyme disease, cowpox, and anthrax. [1] References [ edit ] ^ a b c d e f g Swanson, David L.; Vetter, Richard S. (2006). ... External links [ edit ] Classification D ICD - 10 : T63.3 ICD - 9-CM : 989.5 v t e Poisoning Toxicity Overdose History of poison Inorganic Metals Toxic metals Beryllium Cadmium Lead Mercury Nickel Silver Thallium Tin Dietary minerals Chromium Cobalt Copper Iron Manganese Zinc Metalloids Arsenic Nonmetals Sulfuric acid Selenium Chlorine Fluoride Organic Phosphorus Pesticides Aluminium phosphide Organophosphates Nitrogen Cyanide Nicotine Nitrogen dioxide poisoning CHO alcohol Ethanol Ethylene glycol Methanol Carbon monoxide Oxygen Toluene Pharmaceutical Drug overdoses Nervous Anticholinesterase Aspirin Barbiturates Benzodiazepines Cocaine Lithium Opioids Paracetamol Tricyclic antidepressants Cardiovascular Digoxin Dipyridamole Vitamin poisoning Vitamin A Vitamin D Vitamin E Megavitamin-B 6 syndrome Biological 1 Fish / seafood Ciguatera Haff disease Ichthyoallyeinotoxism Scombroid Shellfish poisoning Amnesic Diarrhetic Neurotoxic Paralytic Other vertebrates amphibian venom Batrachotoxin Bombesin Bufotenin Physalaemin birds / quail Coturnism snake venom Alpha-Bungarotoxin Ancrod Batroxobin Arthropods Arthropod bites and stings bee sting / bee venom Apamin Melittin scorpion venom Charybdotoxin spider venom Latrotoxin / Latrodectism Loxoscelism tick paralysis Plants / fungi Cinchonism Ergotism Lathyrism Locoism Mushrooms Strychnine 1 including venoms , toxins , foodborne illnesses .
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Musical Hallucinations
Wikipedia
Musical hallucinations (also known as auditory hallucinations, auditory Charles Bonnet Syndrome, and Oliver Sacks' syndrome [1] ) describes a neurological disorder in which the patient will hallucinate songs, tunes, instruments and melodies.
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Tracheal Agenesis
Wikipedia
Results were obtained from a total of 32 individual case studies. [11] The classic in-utero symptoms of tracheal agenesis are an absence of the trachea leading to congenital high airway obstruction syndrome, [12] [13] lung distention, polyhydramnios , heart malformations, heart displacement and hydrops fetalis . [1] [12] [14] [15] Other congenital malformations such as genitourinary , gastrointestinal and musculoskeletal anomalies are common and occur in 80% of the reported cases. [16] [11] Tracheal agenesis may lead to a distention of the foetus’ lung due to a build-up of pulmonary fluid within them. ... Neonates with tracheal agenesis present with symptoms characteristic to congenital high airway obstruction syndrome with no audible cry after birth, respiratory insufficiency, respiratory distress and cyanosis . [16] [17] No trachea is palpable below the cricoid cartilage.
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Pseudomyxoma Peritonei
Wikipedia
"New standard of care for appendiceal epithelial neoplasms and pseudomyxoma peritonei syndrome?". Lancet Oncol . 7 (1): 69–76. doi : 10.1016/S1470-2045(05)70539-8 . ... External links [ edit ] Classification D ICD - 10 : C78.6 ICD - 9-CM : 197.6 ICD-O : M8480 MeSH : D011553 DiseasesDB : 31498 External resources eMedicine : med/1795 Orphanet : 26790 v t e Glandular and epithelial cancer Epithelium Papilloma / carcinoma Small-cell carcinoma Combined small-cell carcinoma Verrucous carcinoma Squamous cell carcinoma Basal-cell carcinoma Transitional cell carcinoma Inverted papilloma Complex epithelial Warthin's tumor Thymoma Bartholin gland carcinoma Glands Adenomas / adenocarcinomas Gastrointestinal tract: Linitis plastica Familial adenomatous polyposis pancreas Insulinoma Glucagonoma Gastrinoma VIPoma Somatostatinoma Cholangiocarcinoma Klatskin tumor Hepatocellular adenoma / Hepatocellular carcinoma Urogenital Renal cell carcinoma Endometrioid tumor Renal oncocytoma Endocrine Prolactinoma Multiple endocrine neoplasia Adrenocortical adenoma / Adrenocortical carcinoma Hürthle cell Other/multiple Neuroendocrine tumor Carcinoid Adenoid cystic carcinoma Oncocytoma Clear-cell adenocarcinoma Apudoma Cylindroma Papillary hidradenoma Adnexal and skin appendage sweat gland Hidrocystoma Syringoma Syringocystadenoma papilliferum Cystic, mucinous, and serous Cystic general Cystadenoma / Cystadenocarcinoma Mucinous Signet ring cell carcinoma Krukenberg tumor Mucinous cystadenoma / Mucinous cystadenocarcinoma Pseudomyxoma peritonei Mucoepidermoid carcinoma Serous Ovarian serous cystadenoma / Pancreatic serous cystadenoma / Serous cystadenocarcinoma / Papillary serous cystadenocarcinoma Ductal, lobular, and medullary Ductal carcinoma Mammary ductal carcinoma Pancreatic ductal carcinoma Comedocarcinoma Paget's disease of the breast / Extramammary Paget's disease Lobular carcinoma Lobular carcinoma in situ Invasive lobular carcinoma Medullary carcinoma Medullary carcinoma of the breast Medullary thyroid cancer Acinar cell Acinic cell carcinoma v t e Digestive system neoplasia GI tract Upper Esophagus Squamous cell carcinoma Adenocarcinoma Stomach Gastric carcinoma Signet ring cell carcinoma Gastric lymphoma MALT lymphoma Linitis plastica Lower Small intestine Duodenal cancer Adenocarcinoma Appendix Carcinoid Pseudomyxoma peritonei Colon/rectum Colorectal polyp : adenoma , hyperplastic , juvenile , sessile serrated adenoma , traditional serrated adenoma , Peutz–Jeghers Cronkhite–Canada Polyposis syndromes: Juvenile MUTYH-associated Familial adenomatous / Gardner's Polymerase proofreading-associated Serrated polyposis Neoplasm: Adenocarcinoma Familial adenomatous polyposis Hereditary nonpolyposis colorectal cancer Anus Squamous cell carcinoma Upper and/or lower Gastrointestinal stromal tumor Krukenberg tumor (metastatic) Accessory Liver malignant : Hepatocellular carcinoma Fibrolamellar Hepatoblastoma benign : Hepatocellular adenoma Cavernous hemangioma hyperplasia : Focal nodular hyperplasia Nodular regenerative hyperplasia Biliary tract bile duct : Cholangiocarcinoma Klatskin tumor gallbladder : Gallbladder cancer Pancreas exocrine pancreas : Adenocarcinoma Pancreatic ductal carcinoma cystic neoplasms : Serous microcystic adenoma Intraductal papillary mucinous neoplasm Mucinous cystic neoplasm Solid pseudopapillary neoplasm Pancreatoblastoma Peritoneum Primary peritoneal carcinoma Peritoneal mesothelioma Desmoplastic small round cell tumorMUC2, KRAS, TWIST1, GNAS, MUC5AC, TP53, SERPINA5, MAP2K7, PIK3CB, PIK3CD, PIK3CG, PIK3CA, CXCR6, MUC16, MAPK1, REG4, MAP2K1, PSG2, LPAR2, ACKR3, PTGS2, SSTR4, TOP2A, RNF43, SMUG1, VIM, TLE3, ADRA1A, ADRA2B, COX2, AKT1, ALK, APC, BRS3, CA2, CDH1, CDH2, CEACAM5, CEACAM3, CEACAM7, CTNNB1, EDNRA, EPHB2, FUT8, GPR42, HIF1A, JUN, EPCAM, MCL1, MTCO2P12
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Pituitary Hormone Deficiency, Combined, 2
Omim
Pinto et al. (1997) noted that the finding of 'pituitary stalk interruption syndrome' (PSIS) by MRI is a clinical marker of permanent growth hormone deficiency. ... Affected individuals had similarities to and significant differences from patients with insulin-like growth factor (IGF1; 147440) deficiency due to GH receptor (GHR; 600946) deficiency (see Laron syndrome, 262500), who have normal thyroid function and sexual maturation.PROP1, SOX3, OTX2, GHRH, GNRH1, KISS1R, NR5A1, GNRHR, KISS1, CSHL1, POU1F1, TACR3, GLI2, FGFR1, FGF8, ZIC2, SIX3, PTCH1, SLC20A1, MAGEL2, SHH, SUFU, TDGF1, TGIF1, CDON, LHX3, DLL1, HESX1, PRL, FOXH1, GLI3, GAS1, KIAA0556, GH1, LHX4, NODAL, DISP1, IGF1, BRD2, GHRHR, POMC, FOXA2, PAG1, HHIP, PROK2, RBM28, SMPD3, WDR11, PCBP4, SLC15A4, PROKR2, MIR511, ATP7B, ROBO1, KMT2B, MSH2, CD1A, CREBBP, EIF4E, GHR, GHSR, MSH6, ANOS1, SERPINA1, KMT2D, PITX2, OPN1LW, BMP4, S100A1, S100B, HNF1A, VIM, MIR593
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Motor Neuron Disease
Wikipedia
External links [ edit ] Motor neuron diseases at NINDS Classification D ICD - 10 : G12.2 ICD - 9-CM : 335.2 MeSH : D016472 DiseasesDB : 8358 Wikimedia Commons has media related to Motor neuron diseases . v t e Diseases of the nervous system , primarily CNS Inflammation Brain Encephalitis Viral encephalitis Herpesviral encephalitis Limbic encephalitis Encephalitis lethargica Cavernous sinus thrombosis Brain abscess Amoebic Brain and spinal cord Encephalomyelitis Acute disseminated Meningitis Meningoencephalitis Brain / encephalopathy Degenerative Extrapyramidal and movement disorders Basal ganglia disease Parkinsonism PD Postencephalitic NMS PKAN Tauopathy PSP Striatonigral degeneration Hemiballismus HD OA Dyskinesia Dystonia Status dystonicus Spasmodic torticollis Meige's Blepharospasm Athetosis Chorea Choreoathetosis Myoclonus Myoclonic epilepsy Akathisia Tremor Essential tremor Intention tremor Restless legs Stiff-person Dementia Tauopathy Alzheimer's Early-onset Primary progressive aphasia Frontotemporal dementia / Frontotemporal lobar degeneration Pick's Dementia with Lewy bodies Posterior cortical atrophy Vascular dementia Mitochondrial disease Leigh syndrome Demyelinating Autoimmune Inflammatory Multiple sclerosis For more detailed coverage, see Template:Demyelinating diseases of CNS Episodic/ paroxysmal Seizures and epilepsy Focal Generalised Status epilepticus For more detailed coverage, see Template:Epilepsy Headache Migraine Cluster Tension For more detailed coverage, see Template:Headache Cerebrovascular TIA Stroke For more detailed coverage, see Template:Cerebrovascular diseases Other Sleep disorders For more detailed coverage, see Template:Sleep CSF Intracranial hypertension Hydrocephalus Normal pressure hydrocephalus Choroid plexus papilloma Idiopathic intracranial hypertension Cerebral edema Intracranial hypotension Other Brain herniation Reye syndrome Hepatic encephalopathy Toxic encephalopathy Hashimoto's encephalopathy Both/either Degenerative SA Friedreich's ataxia Ataxia–telangiectasia MND UMN only: Primary lateral sclerosis Pseudobulbar palsy Hereditary spastic paraplegia LMN only: Distal hereditary motor neuronopathies Spinal muscular atrophies SMA SMAX1 SMAX2 DSMA1 Congenital DSMA Spinal muscular atrophy with lower extremity predominance (SMALED) SMALED1 SMALED2A SMALED2B SMA-PCH SMA-PME Progressive muscular atrophy Progressive bulbar palsy Fazio–Londe Infantile progressive bulbar palsy both: Amyotrophic lateral sclerosisSOD1, PNPLA6, PRDX3, VIM, VEGFA, IGHMBP2, VPS54, SOD2, MT3, RHOT1, TARDBP, SNCG, AIF1, OPTN, TBK1, NEK1, FUS, SMN1, SMN2, STMN1, SNRPN, IGFALS, VAPB, ALS2, SNURF, C9orf72, AR, GRN, MAPT, HSPB1, GDNF, IGF1, DCTN1, BSCL2, OGA, NEFH, APOE, SIGMAR1, CHCHD10, SLC1A2, ATXN2, SQSTM1, VCP, CTF1, CHMP2B, DCTN4, VRK1, NEFL, KHDRBS1, DYNC1H1, GTF2H1, NUP62, CNTF, APP, SEMA3A, SLCO6A1, GSTK1, BCL2, SETX, LAS1L, GLE1, HEXB, GEMIN2, GFAP, AAAS, BDNF, ANG, PQBP1, SCAF11, NOP56, LOC643387, CLEC10A, SLC9A3R2, TECPR2, EIF2AK3, ZEB2, FIG4, MFN2, HDAC6, MIR206, GEMIN6, HNRNPA3, UBQLN1, LSM2, C19orf12, PLEKHG5, GJD2, TIGAR, CASC1, TMED9, TMEM106B, TREM2, CDCA5, DCDC2, CHCHD2, ATL1, EXOSC3, UBQLN2, TPPP, LRRK2, AIFM1, PABPC1, NIPA1, HSPB8, PPP1R15A, SIRT1, ARHGEF28, SYNE1, AGTPBP1, SARM1, KIF1B, PARK7, DDX20, NOX1, ACHE, HSPB3, GSTT1, GH1, GLRX, GRIA2, GRM2, GSTM1, GSTP1, HGF, GCHFR, NRG1, HK2, HLA-A, HNRNPA2B1, HP, HRES1, GFRA1, GAP43, IL12A, CDK5, ANXA1, APRT, ASAH1, ATP7A, CAST, CAT, COL17A1, FOXO3, COX8A, DECR1, DSP, EPHA4, FCN2, FKBP1A, HSPB2, INS, CDK5R1, SOS1, RPS6, RRAD, S100B, SLC1A3, SNCA, ACTB, SPAST, RASGRF1, STAT3, TBCE, TIA1, TNF, TP53, UCHL1, RNASE1, RAN, LCN2, NT5E, LY6E, MFAP1, MNAT1, COX1, NAIP, NEFM, PFN1, RAB5A, PIN1, PLS1, PON1, PRPH, PSEN1, PVR, UPK3B
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Adenocarcinoma
Wikipedia
External links [ edit ] Classification D ICD - 9-CM : 151.0 , 182.0 ICD-O : M8140/3 MeSH : D000230 SNOMED CT : 35917007 Media related to Adenocarcinomas at Wikimedia Commons "Adenocarcinoma" —NCI Dictionary of Cancer Terms Surgical Videos, Images and Case Studies of Adenocarcinoma of the Sinuses v t e Glandular and epithelial cancer Epithelium Papilloma / carcinoma Small-cell carcinoma Combined small-cell carcinoma Verrucous carcinoma Squamous cell carcinoma Basal-cell carcinoma Transitional cell carcinoma Inverted papilloma Complex epithelial Warthin's tumor Thymoma Bartholin gland carcinoma Glands Adenomas / adenocarcinomas Gastrointestinal tract: Linitis plastica Familial adenomatous polyposis pancreas Insulinoma Glucagonoma Gastrinoma VIPoma Somatostatinoma Cholangiocarcinoma Klatskin tumor Hepatocellular adenoma / Hepatocellular carcinoma Urogenital Renal cell carcinoma Endometrioid tumor Renal oncocytoma Endocrine Prolactinoma Multiple endocrine neoplasia Adrenocortical adenoma / Adrenocortical carcinoma Hürthle cell Other/multiple Neuroendocrine tumor Carcinoid Adenoid cystic carcinoma Oncocytoma Clear-cell adenocarcinoma Apudoma Cylindroma Papillary hidradenoma Adnexal and skin appendage sweat gland Hidrocystoma Syringoma Syringocystadenoma papilliferum Cystic, mucinous, and serous Cystic general Cystadenoma / Cystadenocarcinoma Mucinous Signet ring cell carcinoma Krukenberg tumor Mucinous cystadenoma / Mucinous cystadenocarcinoma Pseudomyxoma peritonei Mucoepidermoid carcinoma Serous Ovarian serous cystadenoma / Pancreatic serous cystadenoma / Serous cystadenocarcinoma / Papillary serous cystadenocarcinoma Ductal, lobular, and medullary Ductal carcinoma Mammary ductal carcinoma Pancreatic ductal carcinoma Comedocarcinoma Paget's disease of the breast / Extramammary Paget's disease Lobular carcinoma Lobular carcinoma in situ Invasive lobular carcinoma Medullary carcinoma Medullary carcinoma of the breast Medullary thyroid cancer Acinar cell Acinic cell carcinoma v t e Cancer involving the respiratory tract Upper RT Nasal cavity Esthesioneuroblastoma Nasopharynx Nasopharyngeal carcinoma Nasopharyngeal angiofibroma Larynx Laryngeal cancer Laryngeal papillomatosis Lower RT Trachea Tracheal tumor Lung Non-small-cell lung carcinoma Squamous-cell carcinoma Adenocarcinoma ( Mucinous cystadenocarcinoma ) Large-cell lung carcinoma Rhabdoid carcinoma Sarcomatoid carcinoma Carcinoid Salivary gland–like carcinoma Adenosquamous carcinoma Papillary adenocarcinoma Giant-cell carcinoma Small-cell carcinoma Combined small-cell carcinoma Non- carcinoma Sarcoma Lymphoma Immature teratoma Melanoma By location Pancoast tumor Solitary pulmonary nodule Central lung Peripheral lung Bronchial leiomyoma Pleura Mesothelioma Malignant solitary fibrous tumor v t e Digestive system neoplasia GI tract Upper Esophagus Squamous cell carcinoma Adenocarcinoma Stomach Gastric carcinoma Signet ring cell carcinoma Gastric lymphoma MALT lymphoma Linitis plastica Lower Small intestine Duodenal cancer Adenocarcinoma Appendix Carcinoid Pseudomyxoma peritonei Colon/rectum Colorectal polyp : adenoma , hyperplastic , juvenile , sessile serrated adenoma , traditional serrated adenoma , Peutz–Jeghers Cronkhite–Canada Polyposis syndromes: Juvenile MUTYH-associated Familial adenomatous / Gardner's Polymerase proofreading-associated Serrated polyposis Neoplasm: Adenocarcinoma Familial adenomatous polyposis Hereditary nonpolyposis colorectal cancer Anus Squamous cell carcinoma Upper and/or lower Gastrointestinal stromal tumor Krukenberg tumor (metastatic) Accessory Liver malignant : Hepatocellular carcinoma Fibrolamellar Hepatoblastoma benign : Hepatocellular adenoma Cavernous hemangioma hyperplasia : Focal nodular hyperplasia Nodular regenerative hyperplasia Biliary tract bile duct : Cholangiocarcinoma Klatskin tumor gallbladder : Gallbladder cancer Pancreas exocrine pancreas : Adenocarcinoma Pancreatic ductal carcinoma cystic neoplasms : Serous microcystic adenoma Intraductal papillary mucinous neoplasm Mucinous cystic neoplasm Solid pseudopapillary neoplasm Pancreatoblastoma Peritoneum Primary peritoneal carcinoma Peritoneal mesothelioma Desmoplastic small round cell tumor v t e Tumors of the female urogenital system Adnexa Ovaries Glandular and epithelial / surface epithelial- stromal tumor CMS: Ovarian serous cystadenoma Mucinous cystadenoma Cystadenocarcinoma Papillary serous cystadenocarcinoma Krukenberg tumor Endometrioid tumor Clear-cell ovarian carcinoma Brenner tumour Sex cord–gonadal stromal Leydig cell tumour Sertoli cell tumour Sertoli–Leydig cell tumour Thecoma Granulosa cell tumour Luteoma Sex cord tumour with annular tubules Germ cell Dysgerminoma Nongerminomatous Embryonal carcinoma Endodermal sinus tumor Gonadoblastoma Teratoma / Struma ovarii Choriocarcinoma Fibroma Meigs' syndrome Fallopian tube Adenomatoid tumor Uterus Myometrium Uterine fibroids/leiomyoma Leiomyosarcoma Adenomyoma Endometrium Endometrioid tumor Uterine papillary serous carcinoma Endometrial intraepithelial neoplasia Uterine clear-cell carcinoma Cervix Cervical intraepithelial neoplasia Clear-cell carcinoma SCC Glassy cell carcinoma Villoglandular adenocarcinoma Placenta Choriocarcinoma Gestational trophoblastic disease General Uterine sarcoma Mixed Müllerian tumor Vagina Squamous-cell carcinoma of the vagina Botryoid rhabdomyosarcoma Clear-cell adenocarcinoma of the vagina Vaginal intraepithelial neoplasia Vaginal cysts Vulva SCC Melanoma Papillary hidradenoma Extramammary Paget's disease Vulvar intraepithelial neoplasia Bartholin gland carcinoma v t e Tumors of the male urogenital system Testicles Sex cord– gonadal stromal Sertoli–Leydig cell tumour Sertoli cell tumour Leydig cell tumour Germ cell G Seminoma Spermatocytic tumor Germ cell neoplasia in situ NG Embryonal carcinoma Endodermal sinus tumor Gonadoblastoma Teratoma Choriocarcinoma Embryoma Prostate Adenocarcinoma High-grade prostatic intraepithelial neoplasia HGPIN Small-cell carcinoma Transitional cell carcinoma Penis Carcinoma Extramammary Paget's disease Bowen's disease Bowenoid papulosis Erythroplasia of Queyrat Hirsuties coronae glandisTP53, PTGS2, STAT3, PIK3CA, BCL2, CCND1, EGF, PGR, CXCL8, ESR2, MET, ESR1, CDKN2A, STK11, ERBB2, KRAS, KRT20, PPARG, APC, PTEN, PCNA, TP63, EGFR, VEGFA, CTNNB1, RASSF1, MYC, TGFB1, MUC2, GAST, TNF, PLAU, RUNX3, MKI67, ARID1A, KDR, MSLN, SOD2, SPP1, MTOR, NFKB1, BIRC5, PRKD1, OGG1, NR1I2, IL1B, CYP2A6, GPX3, MMP14, CYP19A1, DAPK1, PYCARD, CYP2E1, RARB, FGF9, HOXA10, STAT5A, PTGER1, CASP8, AZGP1, IFNA1, CEACAM1, EFEMP1, PTPN11, UGT2B17, PLCE1, DNMT1, CCN2, HSPD1, TNFRSF10A, PHB, CYP26A1, SELENBP1, NPPA, SERPINA1, TCF7L2, CDKN1C, CKB, GKN1, ID3, KCNQ1, ALOX5, APOA1, DDR1, PRL, APOE, KRT8, CA2, TPM3, ENO1, CYP7B1, PGAM1, KMT2C, TYRP1, GRB7, HRH4, MPP1, HSPA8, NOS3, ACE, FAT4, PAWR, SYCP1, ABL1, CA1, VTI1A, NCOA3, GAGE1, KMT2A, SMARCC1, GHRL, ROBO1, EEF2, RAMP2, GMPR2, ALOX12B, SPHK1, ANGPT2, LTA4H, SIRT1, ERCC1, CAV1, GNAS, UVRAG, VIM, CDKN1B, SATB2, LANCL1, RABEPK, SMUG1, NAPSA, SCLC1, EBNA1BP2, CD274, FGF2, FHIT, FGFR1, CKAP4, CEACAM3, CEACAM7, MIB1, CEACAM5, FOLR1, ARHGEF2, LGR5, CDX2, NQO1, PROM1, CHGA, CD44, CDH1, ERG, H3P10, TYMS, SMAD4, ALDH1A1, ALK, PIK3CB, PIK3CD, MIR21, MIR205, PIK3CG, MAPK1, AR, EPCAM, PSG2, PSMD7, TTF1, KRT7, KLK3, RET, MGMT, AKT1, ABCB1, MLH1, NME1, H3P28, MTCO2P12, MUC6, MUC5AC, MUC4, MUC1, COX2, SERPINE1, MSH2, MRC1, MMP9, MMP7, AFP, MMP2, C17orf97, RPSA, EML4, IL6, BRCA1, HRAS, TFF1, GADL1, HIF1A, AZIN2, SOX2, IGF1, TIMP1, TERT, SLC2A1, IGF2, IL9, S100A2, GSTM1, ARMH1, GSTP1, ROS1, RPE65, BRAF, NKX2-1, S100A4, H3P23, ACTB, TMED7, NFE2L2, CYP1A1, TMED7-TICAM2, NOTCH1, HGF, TICAM2, BRCA2, IFI27, KIT, EPHB2, PSMD9, IGF1R, ZNRD2, FGFR2, DCTN6, XRCC1, CLDN4, GLI1, HSPB1, IGFBP3, CCL2, SST, STMN1, PAX8, DCC, CLDN3, MDM2, NOS2, CDK2, LINC01194, CASP3, CDKN1A, TNFSF10, GSTT1, MSH3, RAF1, KRT5, FSCN1, JAG1, TBC1D9, HSPB3, IL10, SDC1, FLT4, FOLH1, MIA, INSM1, MIR375, FOLR2, MSH6, ABCC1, DPYD, TLR4, TGFBR2, HPGDS, ANXA2, AURKA, DKK3, ETV1, CEACAM6, TIMP3, CLDN7, HSPB2, CADM1, AGR2, MTA1, MIR126, EPAS1, SQSTM1, PDCD1, SERPINB5, CLDN2, FN1, TYMP, FOXM1, MMP1, MIR31, PTGER4, GSTK1, RELA, KIF5B, MIR27A, COL4A5, S100A9, PLAG1, LAT, IFNG, CTNND1, SMARCA4, NTRK1, SFN, ASCL1, MUC16, CXCR4, BSG, HSPA5, TMPRSS2, CA9, SLCO6A1, GABPA, BAX, DCLK1, LEP, EZH2, FBXW7, ERCC2, LGALS3, ERBB3, LMNA, TGM2, HMGA1, ENO2, PROS1, NPEPPS, F3, TSC1, CLDN1, GPC3, SATB1, GATA3, GATA6, SLC7A5, COPD, DYNLL1, STS, EIF3A, WNT5A, SLC2A10, SCGB1A1, PPP1R2C, NOS1, SPARC, CALB2, SLC12A9, CCK, TP73, MAD2L1, FOXA1, ALB, DUSP6, MAPK14, CDH17, E2F1, NRAS, PSAT1, MXI1, WIF1, DSG3, CTSD, MTHFR, AMACR, SFTPB, IL11, USP7, COX1, IL17A, CYLD, IDO1, RUNX2, CLU, GATA4, PLG, ADGRE2, CAT, CFL1, VEGFD, AREG, S100A1, CFTR, DCTN4, PECAM1, MIR34A, IS1, S100A11, S100B, ZHX2, PDX1, SERPINB3, INSR, CTAG1A, MUC3A, IL4, THBS1, CRK, NCAM1, HSP90AA1, TIMP2, NOTCH3, NOTCH2, SYP, XPC, PDCD4, KLF6, TGFA, ARHGAP24, TGFBI, HMOX1, NUP62, HTC2, GTF2H1, CSF1, NTRK3, NTS, ICAM1, SPINK1, SOX4, CTAG1B, HPP1, TRAM1, VEGFC, VHL, CCNE1, XBP1, SI, TNFRSF25, SAI1, FGFR3, FASN, PDPN, HNF4A, SLC16A3, MIR22, APEX1, ETS1, PTGS1, CIB1, EBAG9, IMP3, ZBED1, MDM4, LGALS4, NET1, PDLIM7, PIP, GRAP2, ANXA1, CDH13, TACSTD2, ELF3, ELAVL1, MAPK3, EIF4E, EGR1, DPT, SLC16A4, KHDRBS1, AGER, AKR1B10, CLDN18, HPSE, XIAP, AHR, FAS, MME, MIR155, KLK6, REG1A, SRC, MIR106A, ITGB3, RAD51, PKM, PTCH1, CD109, PGF, PDGFRA, MIR203A, MIR146A, NTSR1, SOX9, MMP13, KLK7, YBX1, NEU1, RRM1, NAT2, POU5F1, MIR192, TMX2-CTNND1, TFF2, ANG, KISS1, SYT1, IL33, GAEC1, MCC, ANPEP, ST14, MCL1, CD24, BMI1, NACC1, MIR210, MYCN, PDGFA, MUC17, LAMC2, MSI1, SFTPA1, PIGR, PTK2, PTMA, MEN1, MIR223, CXCL12, ITGA6, BIRC3, KRT19, MST1R, MSR1, AKT2, KRT18, SCN1A, SCD, SERPINB2, PAK1, MUC5B, ATM, PWAR1, PODXL, MIR224, SOD1, ITGB1, MUTYH, MAGEB6, MIR486-1, SMARCA2, SNAI2, ATP2A3, ALOX15, ADAM8, SLC16A1, AQP1, IGFBP7, SLC2A3, SLC1A5, LCN2, ITGA3, S100P, LDHB, BUB1, TGFB2, CCND2, NEURL1, ETS2, ETV4, HMGB1, F2RL1, GPRC5A, MBD2, SALL4, FGF3, INTS2, MUC3B, FKBP4, FOXO3, SOCS1, COP1, WNK1, CCKBR, IFITM1, NR5A2, LTBP4, BAP1, GORASP1, GALNT3, GAPDH, HMGA2, FOSL1, PSCA, AIMP2, LEPQTL1, GJB1, ADGRE5, RETREG1, CTTN, KEAP1, COL11A1, NOX1, PHGDH, POLDIP2, RNF19A, CSF2, PRAME, MCTS1, CTLA4, CCR7, DICER1, CMA1, PALLD, CYP1A2, CYP1B1, CYP2D6, ANXA10, UBE2C, DDC, DMBT1, DNMT3B, POSTN, AHSA1, GDE1, NDC80, NDRG1, TUBB3, ACSL5, SCO2, XRCC3, F2R, CFLAR, HLA-A, HIC1, VDR, BUB1B, MAP1LC3B, TWIST1, NRG1, CLPTM1L, GUCY2C, MCAT, WT1, CALR, CALCA, SLC52A2, UCHL1, VTCN1, TGFBR1, HSP90B1, CD276, HGD, RIPK3, TLR7, THBS2, CHL1, MIR34C, MIR29B1, MIR29B2, ANGPTL4, SH3GLB1, NES, CYSLTR1, SUB1, METAP2, SSTR3, SSTR2, PLK2, NPRL2, MIR25, PITX1, PLK1, SPA17, MIR200B, PLAGL1, PLA2G4A, PLA2G2A, TSPAN1, CRISP2, CHST4, CDK2AP2, IGF2BP1, SF3B6, TNFRSF1A, OCIAD2, MIR221, LAMTOR5, PRDX4, TLR1, MAGED4B, MIR133B, RPP14, F11R, PAX2, SPZ1, SFTPA2, PRDX2, PPP1R1B, PADI4, REG4, DDR2, LAMTOR2, TMEFF2, SPDEF, BRMS1, TFAP2A, TGFBR3, TG, SLCO1B3, MICA, NPC1, NOTCH4, SGSM3, PALD1, BHLHE22, H3P8, OPA1, SLC22A18, PTP4A3, POTEF, MIR451A, ADIPOR1, FOXP3, POU5F1P3, ERRFI1, SFXN1, DKK1, POU5F1P4, PRDX1, PAEP, PEBP1, P2RX7, OTX2, FAM83A, EPB41L3, CCDC54, OTX1, SNORD118, SYNE1, MAGED4, SETD2, PMS2, SHH, THOC1, RRM2, SAFB, RECK, HHIP, DYRK2, VCAM1, S100A6, CADM4, DDX53, VAV1, BECN1, ABCC3, SLPI, RPL36A, RPL10, H19, LYPD5, SMARCB1, CREB3L4, CIP2A, TNFSF9, ADAM15, TNFRSF6B, NOX5, PLA2G10, PPARD, SEL1L, SHBG, XRCC5, CT83, SFTPD, NAT1, CDCP1, SFTPC, SEMA3B, SFRP1, SELE, SIX1, VIP, SKP2, PDHX, CXCL5, PRSS55, TRPM8, WNT11, SERPINB4, S100PBP, SLC3A2, CSMD1, NANOG, TNFRSF10B, RB1, SOX18, RAB11B, ANO1, MIR148A, PPIG, MIR150, ADIPOQ, SLC52A1, PSEN2, XAF1, ABCG2, PRLR, PDXP, PTGES, TSC2, MIR182, MAP2K7, BCAR1, MAP2K1, MAGI2, XPA, KIF14, MIR200A, CKS1BP7, AURKB, TMPRSS4, PMEPA1, RASA1, IQGAP1, MIR132, NRP1, RARA, ACKR3, CTNNBIP1, RAC1, ZNF582, CHPT1, PTMAP4, UBC, PTK7, DHDDS, PTHLH, TXN, MIR141, MIR145, CCNB2, TTR, SLC28A1, MIR183, ST6GAL1, DPP4, MAL, CCR5, KCNH2, JUN, CKS1B, ATRX, JAK1, FGF1, ITGB4, CISH, FGF7, FGF8, ITGAE, AXL, FKBP5, IRF1, BCHE, INHA, BCL2L1, ING2, ILK, IL18, FOS, CEACAM4, BID, CEL, ABCC2, FAP, COL4A6, LUM, CSTA, ALDH1A3, CSNK2A2, AMELX, CSF1R, AMHR2, CRYZ, SMAD2, CRP, MARCKS, LYZ, ANXA5, PTK2B, ANXA7, LPL, LOXL2, APRT, FASLG, AQP3, LDHA, LAMA3, RHOA, KRT17, KRT15, IL6ST, CDX1, FUS, CD40, HOXA5, GPER1, HOXA1, FOXA2, FFAR2, HLA-G, CASP9, CD40LG, HDAC1, GRN, CCKAR, NR3C1, GNA12, CD34, CD80, CD28, GRP, GSK3B, GSN, GSR, GUCA2A, CD9, GSTA1, GSTM3, CAMP, GLI3, BMP7, IFNA13, CCN1, BNIP3, CDK4, IGFBP5, IGFBP4, IGFBP2, IGFBP1, GCG, CDH3, GCNT1, IFNA17, IFNA2, CD63, IFN1@, IDH1, CDC25A, GGT1, GHRH, CA8, HSD11B1, HES1, HPGD, CD68, CALCR, AGTR1, ATOH1, MAOA, NFIB, CX3CR1, MYOD1, DECR1, MYCL, MCM2, MCM5, ACP3, CYP2A13, MDK, ELANE, MTAP, ADH5, MFAP1, MST1, CD99, E2F4, MMP3, DAG1, DAB2, CYP27B1, CYP24A1, ADM, MMP12, MARK2, NFYA, CTSE, DHCR24, NM, CTSB, NFKBIA, SLC26A3, ADRB2, AICDA, IGAD1, DLD, CD86, SPINT2, C21orf58, RAB32, COPS5, A4GALT, DUOX1, FAM3B, CDH2, TLR9, DCUN1D1, PTOV1, AKR1C2, CDC6, CEMIP, DDT, CDC5L, SMOX, ING3, DLL4, CDK1, TRIM44, PPP1R12C, MS4A3, DAXX, VAX1, IL17D, IL24, PSIP1, S100A14, CDKN2B, BPIFA1, NUDT6, TNFRSF12A, ZBTB7A, WT1-AS, ZMYND10, CORO1A, MAGEC2, GULP1, DCDC2, LIMA1, ISYNA1, GTSE1, CDK6, RCAN3, NBAS, CD55, CDH12, CDH10, SOX30, OGFR, RTEL1, CDK12, SIDT1, TRPM7, MKS1, RNF43, MAP3K2, CHFR, ZNF415, NUP107, ADCY10, NOXA1, CAND1, HSPH1, RAB25, KMT2E, SEPTIN9, SULF2, MYDGF, DEFA1, CD59, DIABLO, CD47, PNPLA2, SLC2A4RG, RAD18, C1GALT1, LXN, DEFA5, AHCYL1, OTUD7B, TIMM8A, PLAC1, GSDME, STAG2, CD38, ATF7IP, PGRMC1, TENM3, BRD8, DLL3, RAB40B, NSD3, CDA, CD151, PTGES3, AKIRIN2, MAP1S, TMED2, RALBP1, PACC1, LZTS1, PELI1, ZNF654, CCDC88A, SMR3B, LAPTM4B, ADAM28, TRPV6, RTN4, KLK15, ITLN1, SLC26A1, RAB20, NLRP2, HIF1AN, KDM4D, NSUN5, DDX3X, CYP17A1, CES1, ATF2, PLA2G2D, CREB1, EPC2, DCAF4, KLK13, CXADR, KDM4B, INTS6, PEG10, SNED1, KRT23, PHF8, WWTR1, CLIC4, CNNM4, MYEOV, LEF1, PPA2, ACIN1, COX8A, DKK4, BBC3, FOXP1, LAMP3, ANKRD1, GREM1, PELP1, CPB2, CRABP2, PLCH1, ATP2C1, CKAP2, NELFB, RCHY1, CREBBP, SIRT4, CSE1L, PPP1R13B, UFL1, CASP14, PRG1, CHST5, SEC14L2, CTSZ, ANP32C, HEY2, CBX7, CTNND2, CBX5, HEY1, CTSK, ARFIP2, CTSL, TRIM29, PHLPP1, PRKD3, CRMP1, IL17RA, PLCB1, JMJD6, CRHR1, TNFAIP8, KLK5, LARP4B, RGL1, CREM, PRKD2, COX7A1, INTU, IL17B, NOX4, CHUK, PNPLA8, POLI, ANO7, IL22, KLK8, AKAP13, KLK14, DUSP10, DUOX2, PLA2G3, RPL35, RRM2B, GALNT6, STMN3, CHRNB4, CHRNA5, TXNDC12, CHRNA4, CHEK2, CYP11B2, CHRM3, APH1A, ZDHHC9, CHI3L1, A4GNT, COMMD3, ING4, JPT1, EGFL7, PTENP1, KLK12, STOML2, MAP3K8, CNTN1, DROSHA, LTB4R, REM1, KIDINS220, TRIB2, CDH20, COL1A2, CTAG2, COL3A1, SIRT2, COL17A1, COMT, CRCP, SRPX2, ATF6, CCR4, KLRK1, CLIC1, RPH3A, SLC39A3, CYP3A4, NOP53, LMTK2, FSCN3, MGLL, HUNK, ERVW-1, TUSC2, ZNRD1, ACOT7, PARK7, PPM1H, NOP2, MTA3, APOBEC1, MIR214, ALOX15B, AMFR, MIR200C, AMPD1, AMY1A, MIR196A1, MIR193A, AMY1B, AMY1C, ANGPT1, MIR17, MIR15A, ANXA4, APAF1, APBA1, MIR142, MIR217, ALOX12, ALDH1B1, MIR96, ADORA2B, POTEKP, ZYG11A, PRKCQ-AS1, PIM3, MIR17HG, MIR98, PARP1, ALDH2, AP2A1, AGT, MIR29A, NR0B1, AK2, MIR23B, MIR23A, APBA2, APP, MIR196B, MIR106B, PGP, OR10A4, NEAT1, ARL2, MAGEA2B, ARRB2, MAGI3, ARSA, IL4I1, GK5, CASC2, RICTOR, IL27, ATF4, FAM83B, TMED4, ALKBH3, ARHGDIB, TUSC7, CAGE1, AMIGO2, MIR100, MIRLET7G, USP17L9P, ACF, USP17L2, ABCC6, ARAF, SOX2-OT, TRIM59, MACC1, ACTBL2, EVX2, RSPO2, ARG1, TAS2R64P, S100A7A, MIR135B, CT45A1, MAVS, MIR944, COMMD3-BMI1, ACP1, RPL17-C18orf32, SNHG16, OCLN, MIR3662, MIR642B, HOTTIP, ALL2, ACTG1, MIR1290, MIR1297, MIR1206, MIR1288, ACTG2, SYCE1L, VPS9D1-AS1, MIR499B, MIR4735, MED4-AS1, ACR, H3P47, H3P42, SERPINA3, ABO, ACAT1, LOC110806263, PANCR, LINC01614, SYNPR-AS1, TP53COR1, GATD3B, LOC102723971, SATB1-AS1, PGR-AS1, APOBEC3A_B, STEAP2-AS1, ACTN4, MIR938, MIR363, ACVR1B, NME1-NME2, GGTLC5P, ADH1C, NCF1, ANXA8, ADH4, POTEM, ADH7, MIR483, DEFA1A3, MIR503, MIR499A, MIR498, MIR193B, MIR495, MIR511, ADK, MIR487B, MIR542, MIR625, USP17L26, GGTLC4P, ACVRL1, GGT2, USP17L30, USP17L29, USP17L28, USP17L27, ADA, ADCYAP1R1, USP17L25, USP17L24, DEFA1B, ADAR, GGTLC3, ANXA8L1, ADCYAP1, ZEB1-AS1, TBCEL, CCNY, MUL1, TNKS2, ULBP1, CPEB4, EPC1, TET1, CDK5RAP3, PTGES2, NAA25, WLS, CALM1, CALM2, LPCAT1, RABEP2, CAMKMT, PALB2, LIN28A, CALM3, PDCD1LG2, CA11, SRCIN1, BTF3, CTTNBP2, FSD1L, YPEL3, MS4A8, TEX101, SOX7, NUF2, SHARPIN, ITIH5, VANGL1, BTK, APOLD1, C1QBP, SLC38A1, FMNL1, COL18A1, ADIPOR2, CAPG, ATP12A, CDC73, SEMA4A, ABCG4, ALX4, HPSE2, ELOVL5, LGR6, CCNA2, EVA1C, CCNB1, NGB, CCND3, ANKRD36B, RDH14, CD3E, KLHL1, MTUS1, MS4A1, RHBDF1, SOX17, KRIT1, FRTS1, PAGR1, BIRC7, IGF2BP3, FSD1, PRR15L, FA2H, BOLL, CASR, ZMAT3, MARCKSL1, PINK1, RUNX1, GINS3, CBFB, CBR1, CBS, ZFP36L1, TMPRSS13, EVA1A, BRDT, OR2AG1, BAGE, ROMO1, GATA5, BAK1, RAET1E, BCL2L2, IL31RA, AASDH, BDNF, SLC43A2, MSI2, NOXO1, CYP2R1, PRAP1, SCGB3A2, DNTTIP1, BAG1, NLRP4, BAD, PAOX, SAMD14, FLCN, LIPH, GKN2, APOBEC3A, CRTC2, ATP5F1B, RASSF6, SIK1, AVP, CBLL2, AGR3, MARVELD2, BTLA, CCDC80, GPBAR1, TNFRSF13C, UHRF2, GBP5, FOXL2, SNORD14B, BAGE4, RIOX2, LINC00525, ZNF577, DST, KDM2B, MAP1LC3A, SNORD14D, SNORD35B, SRRM4, MAML2, MIEN1, ING5, MINDY4, ANTXR1, SNORD14C, SNORD14E, KCTD12, FOXQ1, STK11IP, CARD16, NLRP3, UCN3, TMEM54, CXCR5, SAT2, BMP2, SLC45A3, BMP4, CRB3, STRADA, CTU1, RHOT2, ABCC10, LMLN, CASP2, PDZK1IP1, DMP1, IRF3, IL15RA, TNFRSF9, SDHB, CX3CL1, ING1, CCL21, CCL17, CCL16, CCL5, CCL3, CCL1, SCTR, SCT, SCN7A, INHBA, INS, EIF3E, MAP2K4, SFPQ, IL13, SHMT1, IGKC, IGSF1, IHH, SIX3, IKBKB, IL1A, IL1RN, IL5, SFRP2, CXCR2, IL11RA, IL12B, TRA2B, SRSF5, SFRP5, SFRP4, SAT1, IRS1, IGFBP6, SAA2, SNORD15A, RNASE3, RGS1, RFX1, TRIM27, KLK2, REN, KLC1, KIFC1, RECQL, RBP1, RBL2, RBBP6, KRT4, KRT6A, PLAAT4, RARG, KCNJ3, ROCK1, RORA, ITGAV, SAA1, ITGA2, ITGA4, S100A10, ITGAL, S100A8, S100A7, ITGB2, CD82, EIF6, RTN1, JAG2, RREB1, RPS23, JAK2, RPL17, SLC2A4, SLC4A1, HDGF, HSD17B1, TCTE3, TRG, TCP1, TCN1, TCF21, HOXB7, HNF1B, TCF4, TBP, TBX1, TAGLN, TBXT, HOXD@, HP, AURKC, STIM1, STAT6, HOXB@, TMBIM6, TEK, HLA-DQB1, THY1, THRB, THBS4, CFH, HGFAC, HLA-C, HLA-DQA1, HMGCR, TERC, LEFTY2, HNRNPU, HOXA4, TFF3, HOXA7, HOXA9, HOXA11, STAT5B, HSPA1A, SLC5A1, STAT1, SNCA, SNAP25, SNAI1, SMO, IFNGR1, IGBP1, IGF2R, HLTF, SMARCA1, SLC19A1, SLC18A1, SLC12A2, SLC12A1, SLC6A8, SLC6A3, SLC5A5, SLC5A2, SOAT1, IDH2, SOX11, SSTR1, HSPA1B, ST13, SS18, SSTR5, SSTR4, HSPA2, HSPA4, HSPA9, ID4, HSPE1, SPRR3, SPRR1B, TNC, SPOCK1, SPINT1, ID1, KRT13, KRT14, RAD52, PAX5, PFKP, PFKM, PFKFB3, PENK, SERPINF1, MMP8, PDYN, PDK2, PDGFRB, PDGFRL, MMP17, PDE4D, PDE3A, PDCD2, MMP19, CD200, PCCB, PFN1, PGD, MIF, PIK3R1, MCAM, PLA2G1B, PKP2, PKP1, PITX2, CD46, PIK3R2, ME1, MGP, PIM1, MECP2, MEF2C, MAP3K5, SERPINE2, SCGB2A2, KITLG, PCCA, MPO, MOK, PAX1, NR4A2, MYH9, NAGLU, ROR2, ROR1, NAIP, NTRK2, RPL10A, NT5E, NRL, NFKB2, NPAS2, CCN3, NGF, NGFR, NHLH1, NNAT, ODC1, OLR1, MYB, MT3, MRE11, PRKN, PAM, MSMB, MSN, MSRA, MT1B, PA2G4, OPCML, P2RX5, P2RX4, ATP6, MTR, ORM1, MUC7, OPRD1, MBD1, MB, MAX, PLAT, PTGIS, PTGFR, LDLR, PTGER3, PTGER2, LIG4, LNPEP, LOX, PSPH, PSME2, LPA, LRP1, PSEN1, KLK10, LTA, TMPRSS15, LYN, LBR, LAMP1, LAMB1, PTPRJ, KRT16, RAD21, PYGB, PXN, NECTIN1, PVR, PTPRZ1, PTPRF, PTK6, PTPRB, KRT81, QSOX1, PTN, PTMS, L1CAM, LAG3, PRNP, MXD1, MAP2K5, MAS1, POR, PON1, POMC, PMP22, PML, PLXNB1, PLXNA1, MAT1A, MAGEA4, PLEC, PLCG1, PLCB4, PLCB3, PLCB2, PLAUR, MAT2A, POU3F2, PPA1, MAP2K2, PRKAA2, SMAD1, MAPK7, SMAD3, PRKCZ, SMAD7, PRKCI, PRKAB1, PRKAA1, PPARA, PTPA, PPP2CB, PPP1R1A, PPM1A, MED1, MAGEA1, MAGEA2, KLF10, HDAC2, ATN1, EXO1, TRIP10, TRIP13, KLF4, CD83, EPOR, IL32, PTTG1, ERBB4, XPR1, EREG, ZMYM4, EYA4, SLC33A1, SLC16A7, ERCC4, ERCC5, TMSB10, SLC9A3R2, EPO, KL, HAND2, CXCL14, EMX2, EN2, GAL3ST1, ENG, ROCK2, ATG5, FHL5, NRXN3, EIF2AK3, CHST2, EP300, EPHA3, LPXN, EPHA4, EPHX2, ESA4, ESRRA, GTF2IRD1, DYRK1B, FANCC, FANCD2, MGAM, SKAP2, ACSL4, MBD4, BCL10, FANCG, ARHGEF7, IER3, APLN, FAU, CCN4, CCN5, FBN2, GGH, FCGR3A, SOCS3, SPAG9, DOK2, EXT1, ESRRG, ATG12, CBFA2T2, ARHGEF1, ETFA, SMC3, ETV6, EYA2, ARTN, RGN, USP8, FAAH, FABP4, CLDN6, NFS1, FABP3, CHD1L, CLOCK, HBE1, NME2, RACK1, DVL1, E2F2, CNPY2, AKR1A1, CRISP3, B3GALT5, E2F3, PAK4, ECT2, LPAR1, EEF1A2, EEF1B2P2, CTDSPL, RBM5, TENM1, EEF1G, PIAS3, DUSP2, YAP1, GLRX3, CDC42EP3, DSC1, IFITM2, DSC2, DSC3, DSP, ANP32B, HBEGF, SPON2, ATG7, DEAF1, DUSP1, CAP1, TACC3, PGRMC2, PRMT5, ATP6AP2, NAMPT, APOBEC3B, TRAP1, ZEB2, MELK, SPATA2, RASSF2, PCLAF, HDAC4, KMT2B, SETD1A, HDAC9, KDM4A, PHF14, EIF5B, ISG15, CLCA2, KLK4, RIN1, CARTPT, EIF5A, PAN2, MFN2, DNAJB6, FRY, LRPPRC, RAD50, EFNA1, ACTR3, EDIL3, ABCF2, FRAT1, EIF4EBP1, ZBTB33, ABI1, EFNB1, CASP8AP2, EPHA2, NR1H4, MVP, NRP2, FCGR3B, CES2, GRM1, VIPR1, CXCR3, GPR39, GRK5, GPT, GPX1, GPX4, GRIA2, KDM6A, USF2, USF1, UQCRFS1, UPK2, COL14A1, UGT8, UGT1A, UCP2, VRK1, VTN, WARS1, GLI2, ZNF124, ZFY, YES1, GCLC, XRCC4, GCLM, XRCC2, GLP1R, LAT2, XBP1P1, GLS, GOT2, WNT8B, GPC1, WNT1, CORO2A, UCN, UBE2N, INPP4B, UBE2I, H2AX, TOP2A, TNNI3, TNNC1, TNFRSF1B, HABP2, HAGH, CLEC3B, CLDN5, HAS1, TLR5, HAS2, TLR3, TLR2, HAS3, TKT, TK1, GYPA, TPI1, GUCA2B, TSG101, GRM3, U2AF1, TYRO3, PDIA3, TXNRD1, GSS, TSHR, TRPM2, TPTE, TRIO, CCT3, TRG-TCC1-1, TRG-GCC2-6, TRNAG1, TRAF1, GTF2H4, TRIM25, PTP4A1, GJA1, GIP, AKR1C3, AOC3, FLT3, RFXANK, PSMG1, CDK13, TNFSF11, PRKRA, KHSRP, API5, BARX2, DGKZ, FPR1, CNTNAP1, CUL2, DOC2A, FRA16D, FLT1, PDE5A, FOXO1, FGF13, FGF18, FDFT1, TNFRSF10C, FADD, FGF5, CD164, ADAM9, TNFSF13, TNKS, RIPK1, FGFR4, B3GALT1, HYAL2, FOXF1, FOXC2, IRS2, RASAL1, FRZB, SRPX, ARHGEF5, MFAP5, PTP4A2, CUL5, GDF9, GFAP, ADAM12, CCDC6, TFPI2, FXR1, B4GALT1, TFEB, DEK, GH1, GHR, SCG2, GHRHR, KMT2D, GPR68, SPOP, RBM10, FUT4, PLA2G6, FYN, AXIN1, G6PD, EPX, TKTL1, USP9X, ANP32A, DVL1P1, GATD3A, NRIP1, XRCC6, MLRL, GALNS, ST8SIA2, A1BG
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Hand Eczema
Wikipedia
External links [ edit ] Classification D ICD - 10 : L20 L23 L24 L25 L30 v t e Dermatitis and eczema Atopic dermatitis Besnier's prurigo Seborrheic dermatitis Pityriasis simplex capillitii Cradle cap Contact dermatitis ( allergic , irritant ) plants: Urushiol-induced contact dermatitis African blackwood dermatitis Tulip fingers other: Abietic acid dermatitis Diaper rash Airbag dermatitis Baboon syndrome Contact stomatitis Protein contact dermatitis Eczema Autoimmune estrogen dermatitis Autoimmune progesterone dermatitis Breast eczema Ear eczema Eyelid dermatitis Topical steroid addiction Hand eczema Chronic vesiculobullous hand eczema Hyperkeratotic hand dermatitis Autosensitization dermatitis / Id reaction Candidid Dermatophytid Molluscum dermatitis Circumostomy eczema Dyshidrosis Juvenile plantar dermatosis Nummular eczema Nutritional deficiency eczema Sulzberger–Garbe syndrome Xerotic eczema Pruritus / Itch / Prurigo Lichen simplex chronicus / Prurigo nodularis by location: Pruritus ani Pruritus scroti Pruritus vulvae Scalp pruritus Drug-induced pruritus Hydroxyethyl starch-induced pruritus Senile pruritus Aquagenic pruritus Aquadynia Adult blaschkitis due to liver disease Biliary pruritus Cholestatic pruritus Prion pruritus Prurigo pigmentosa Prurigo simplex Puncta pruritica Uremic pruritus Other substances taken internally: Bromoderma Fixed drug reaction Nummular dermatitis Pityriasis alba Papuloerythroderma of Ofuji
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Fatal Insomnia
Wikipedia
"Sporadic fatal insomnia masquerading as a paraneoplastic cerebellar syndrome" . Arch. Neurol . 65 (7): 971–973. doi : 10.1001/archneur.65.7.971 . ... External links [ edit ] Classification D ICD - 10 : A81.9 ICD - 9-CM : 046.72 OMIM : 600072 MeSH : D034062 DiseasesDB : 32177 "AFIFF Fatal Familial Insomnia Families Association" . v t e Prion diseases and transmissible spongiform encephalopathy Prion diseases in humans inherited/ PRNP : fCJD Gerstmann–Sträussler–Scheinker syndrome Fatal familial insomnia sporadic: sCJD Sporadic fatal insomnia Variably protease-sensitive prionopathy acquired/ transmissible: iCJD vCJD Kuru Prion diseases in other animals Bovine spongiform encephalopathy Camel spongiform encephalopathy Scrapie Chronic wasting disease Transmissible mink encephalopathy Feline spongiform encephalopathy Exotic ungulate encephalopathy
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Dysgraphia
Wikipedia
The disorder generally emerges when the child is first introduced to writing. [2] Adults, teenagers, and children alike are all subject to dysgraphia. [5] Dysgraphia should be distinguished from agraphia , which is an acquired loss of the ability to write resulting from brain injury , stroke , or progressive illness. [6] Contents 1 Classification 1.1 Dyslexic 1.2 Motor 1.3 Spatial 2 Signs and symptoms 2.1 Associated conditions 3 Causes 4 Diagnosis 5 Treatment 6 School 7 See also 8 References 9 Further reading 10 External links Classification [ edit ] Dysgraphia is nearly always accompanied by other learning disabilities such as dyslexia or attention deficit disorder , [2] [7] [8] and this can impact the type of dysgraphia a person might have. Tourette’s syndrome and ASD are other common problems among dysgraphic individuals. [9] There are three principal subtypes of dysgraphia that are recognized. ... NINDS Dysgraphia Information Page v t e Dyslexia and related specific developmental disorders Conditions Speech, language , and communication Expressive language disorder Infantile speech Landau–Kleffner syndrome Language disorder Lisp Mixed receptive-expressive language disorder Specific language impairment Speech and language impairment Speech disorder Speech error Speech sound disorder Stuttering Tip of the tongue Learning disability Dyslexia Dyscalculia Dysgraphia Disorder of written expression Motor Developmental coordination disorder Developmental verbal dyspraxia Sensory Auditory processing disorder Sensory processing disorder Related topics Dyslexia research Irlen filters Learning Ally Learning problems in childhood cancer Literacy Management of dyslexia Multisensory integration Neuropsychology Reading acquisition Spelling Writing system Lists Dyslexia in fiction Languages by Writing System People with dyslexia
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Spastic Cerebral Palsy
Wikipedia
Some people with this type of CP can accomplish activities of daily living independently, while some need the assistance of a personal care aide for certain tasks, and others need 24-hour support. [21] About 1/3 of people with cerebral palsy cannot walk, about 1/2 have intellectual disabilities, and 3/4 experience some level of chronic pain. [21] There is limited research on adults with spastic CP. [22] The brain injury causing CP does not progress or change, but the functional impact and thus, one's needs may change with age. [7] Some issues specific to adults with spastic and other forms of cerebral palsy are: Premature aging [8] Fatigue [8] Pain [8] Arthritis [8] Depression and anxiety [8] Post impairment syndrome [8] Regardless of their particular expression of spastic cerebral palsy, affected individuals can lead fulfilling lives. ... External links [ edit ] Classification D ICD - 10 : G80 ICD - 9-CM : 343 v t e Cerebral palsy Symptoms and signs Spasticity Upper motor neuron lesion Spastic cerebral palsy Scissor gait Spastic diplegia Spastic hemiplegia Spastic quadriplegia Ataxia and others Ataxic cerebral palsy Dyskinetic cerebral palsy Diagnosis General movements assessment Measurement scales Gross Motor Function Classification System - Expanded & Revised (gross motor function) Manual Ability Classification System (manual dexterity) Communication Function Classification System (communication) Modified Ashworth scale (spasticity) Management Management of cerebral palsy Selective percutaneous myofascial lengthening Rhizotomy Other People with cerebral palsy Cerebral palsy organizations Works about cerebral palsy and other paralytic syndromes v t e Medicine Specialties and subspecialties Surgery Cardiac surgery Cardiothoracic surgery Colorectal surgery Eye surgery General surgery Neurosurgery Oral and maxillofacial surgery Orthopedic surgery Hand surgery Otolaryngology ENT Pediatric surgery Plastic surgery Reproductive surgery Surgical oncology Transplant surgery Trauma surgery Urology Andrology Vascular surgery Internal medicine Allergy / Immunology Angiology Cardiology Endocrinology Gastroenterology Hepatology Geriatrics Hematology Hospital medicine Infectious disease Nephrology Oncology Pulmonology Rheumatology Obstetrics and gynaecology Gynaecology Gynecologic oncology Maternal–fetal medicine Obstetrics Reproductive endocrinology and infertility Urogynecology Diagnostic Radiology Interventional radiology Nuclear medicine Pathology Anatomical Clinical pathology Clinical chemistry Cytopathology Medical microbiology Transfusion medicine Other Addiction medicine Adolescent medicine Anesthesiology Dermatology Disaster medicine Diving medicine Emergency medicine Mass gathering medicine Family medicine General practice Hospital medicine Intensive care medicine Medical genetics Narcology Neurology Clinical neurophysiology Occupational medicine Ophthalmology Oral medicine Pain management Palliative care Pediatrics Neonatology Physical medicine and rehabilitation PM&R Preventive medicine Psychiatry Addiction psychiatry Radiation oncology Reproductive medicine Sexual medicine Sleep medicine Sports medicine Transplantation medicine Tropical medicine Travel medicine Venereology Medical education Medical school Bachelor of Medicine, Bachelor of Surgery Bachelor of Medical Sciences Master of Medicine Master of Surgery Doctor of Medicine Doctor of Osteopathic Medicine MD–PhD Related topics Alternative medicine Allied health Dentistry Podiatry Pharmacy Physiotherapy Molecular oncology Nanomedicine Personalized medicine Public health Rural health Therapy Traditional medicine Veterinary medicine Physician Chief physician History of medicine Book Category Commons Wikiproject Portal Outline v t e Neuroscience Outline of neuroscience History of neuroscience Basic science Behavioral epigenetics Behavioral genetics Cellular neuroscience Computational neuroscience Connectomics Imaging genetics Integrative neuroscience Molecular neuroscience Neural engineering Neuroanatomy Neurochemistry Neuroendocrinology Neurogenetics Neuroinformatics Neurometrics Neuromorphology Neurophysics Neurophysiology Systems neuroscience Clinical neuroscience Behavioral neurology Clinical neurophysiology Neurocardiology Neuroepidemiology Neurogastroenterology Neuroimmunology Neurointensive care Neurology Neurooncology Neuro-ophthalmology Neuropathology Neuropharmacology Neuroprosthetics Neuropsychiatry Neuroradiology Neurorehabilitation Neurosurgery Neurotology Neurovirology Nutritional neuroscience Psychiatry Cognitive neuroscience Affective neuroscience Behavioral neuroscience Chronobiology Molecular cellular cognition Motor control Neurolinguistics Neuropsychology Sensory neuroscience Social cognitive neuroscience Interdisciplinary fields Consumer neuroscience Cultural neuroscience Educational neuroscience Evolutionary neuroscience Neuroanthropology Neurobioengineering Neurobiotics Neurocriminology Neuroeconomics Neuroepistemology Neuroesthetics Neuroethics Neuroethology Neurohistory Neurolaw Neuromarketing Neuromorphics Neurophenomenology Neurophilosophy Neuropolitics Neurorobotics Neurotheology Paleoneurobiology Social neuroscience Concepts Brain–computer interface Neural development Neural network (artificial) Neural network (biological) Detection theory Intraoperative neurophysiological monitoring Neurochip Neurodegeneration Neurodevelopmental disorder Neurodiversity Neurogenesis Neuroimaging Neuroimmune system Neuromanagement Neuromodulation Neuroplasticity Neurotechnology Neurotoxin Book Category
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Hereditary Folate Malabsorption
Wikipedia
There can be (i) pancytopenia , (ii) diarrhea and/or mucositis and/or (iii) immune deficiency due to T-cell dysfunction and hypoimmunoglobulinemia resulting in pneumonia usually due to Pneumocystis jirovecii . [1] Recently, several infants with the immune deficiency syndrome were described. [2] [3] [4] Untreated, or with inadequate treatment, there are progressive systemic and neurological signs with a spectrum of manifestations including seizures that are often intractable. ... Differential diagnosis [ edit ] HFM must be distinguished from cerebral folate deficiency (CFD)– a syndrome in which there is normal intestinal folate absorption, without systemic folate deficiency, but a decrease in CSF folate levels.
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Cerebral Arteriovenous Malformation
Wikipedia
The point prevalence in adults is approximately 18 per 100,000. [2] AVMs are more common in males than females, although in females pregnancy may start or worsen symptoms due to the increase in blood flow and volume it usually brings. [23] There is a significant preponderance (15-20%) of AVM in patients with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome). [22] Research directions [ edit ] No randomized, controlled clinical trial has established a survival benefit for treating patients (either with open surgery or radiosurgery) with AVMs that have not yet bled. [24] References [ edit ] ^ "Oculomotor neuropathy from an unruptured arteriovenous malformation in the frontal operculum: A case report" . ... The Aneurysm and AVM Foundation (TAAF) v t e Congenital vascular defects / Vascular malformation Great arteries / other arteries Aorta Patent ductus arteriosus Coarctation of the aorta Interrupted aortic arch Double aortic arch Right-sided aortic arch Overriding aorta Aneurysm of sinus of Valsalva Vascular ring Pulmonary artery Pulmonary atresia Stenosis of pulmonary artery Subclavian artery Aberrant subclavian artery Umbilical artery Single umbilical artery Great veins Superior / inferior vena cava Congenital stenosis of vena cava Persistent left superior vena cava Pulmonary vein Anomalous pulmonary venous connection ( Total , Partial ) Scimitar syndrome Arteriovenous malformation Cerebral arteriovenous malformation
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Schwannomatosis
Gene_reviews
Kehrer-Sawatzki et al [2017] Clinical Characteristics Clinical Description Schwannomatosis is an autosomal dominant tumor suppressor syndrome with reduced penetrance, characterized by a predisposition to develop multiple schwannomas (histologically benign nerve sheath tumors) and much less frequently meningiomas [Merker et al 2012]. ... Malignant transformation of schwannomas remains a theoretic risk as in other tumor suppressor syndromes [Evans et al 2012]. Malignant schwannomas were identified in two individuals with clinically diagnosed familial schwannomatosis [Gonzalvo et al 2011].
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Spinocerebellar Ataxia Type 14
Gene_reviews
Identification of PRKCG pathogenic variants in persons with phenotypes similar to progressive myoclonic ataxia (Ramsay Hunt syndrome) [Visser et al 2007] and myoclonus-dystonia [Foncke et al 2010] suggest that SCA14 should be considered in individuals with these clinical syndromes.
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Thyroid Nodule
Wikipedia
External links [ edit ] Classification D ICD - 10 : E04.1 ICD - 9-CM : 241.0 MeSH : D016606 DiseasesDB : 5332 SNOMED CT : 237495005 External resources MedlinePlus : 007265 eMedicine : med/3224 v t e Thyroid disease Hypothyroidism Iodine deficiency Cretinism Congenital hypothyroidism Myxedema Myxedema coma Euthyroid sick syndrome Signs and symptoms Queen Anne's sign Woltman sign Thyroid dyshormonogenesis Pickardt syndrome Hyperthyroidism Hyperthyroxinemia Thyroid hormone resistance Familial dysalbuminemic hyperthyroxinemia Hashitoxicosis Thyrotoxicosis factitia Thyroid storm Graves' disease Signs and symptoms Abadie's sign of exophthalmic goiter Boston's sign Dalrymple's sign Stellwag's sign lid lag Griffith's sign Möbius sign Pretibial myxedema Graves' ophthalmopathy Thyroiditis Acute infectious Subacute De Quervain's Subacute lymphocytic Palpation Autoimmune /chronic Hashimoto's Postpartum Riedel's Enlargement Goitre Endemic goitre Toxic nodular goitre Toxic multinodular goiter Thyroid nodule Colloid noduleDICER1, PTEN, PTCH1, BRAF, TRPM3, CCDC6, TSHR, TG, RET, TAS2R38, APC, F9, CALCA, LGALS3, ACR, TPO, SMUG1, SLC5A5, KRAS, IGF1, PPARG, NRAS, HT, ECM1, TGFB1, NCOA4, HMGA2, TERT, LOC110806263, CXCR6, TMPRSS4, ORI6, NKX2-1, ALPI, ALB, PTGS2, ALPP, PAX8, NTRK1, CD47, MMP2, GDF15, IAPP, HRAS, CD274, TFF3, FOLH1, SLCO6A1, MAGT1, GSTK1, MIRLET7G, GSC, MIR4306, XRCC1, VEGFA, UROD, GADL1, TTF1, ACKR3, MIR146B, MIR145, TPM3, TP53, MTCO2P12, MIR183, MIR197, ALK, TFPI, DLG1-AS1, GRK2, KIDINS220, MIR21, SHC3, ADRA1A, FLVCR1, MIR221, AZIN2, MIR95, QPRT, ADRA2B, RASSF1, PPP1R13L, MIR199A1, NIBAN1, MIR196B, GSTO1, LPAR2, MIR485, FOSL1, MIR199A2, CCND1, STRN, ERBB2, SFN, GNB3, GHR, GH1, GFRA1, GDF1, GATA3, FOXE1, FAP, APP, ETV6, ETS1, EIF1AX, GSTM1, EGFR, EDNRA, DPP4, CYP1A1, CLU, CHGA, CEACAM5, TNFSF8, TNFRSF8, AR, BRS3, ARRB2, GPR42, GSTP1, SSTR4, NCAM1, SSTR2, SST, HLTF, SHBG, BMP1, PTPN11, PTN, PTH, ADCY6, ANGPT2, PPP3R1, SLC26A4, COX2, GSTT1, MT1A, BIRC5, LEP, KRT19, KIT, KCNJ6, ITGA6, IL6R, IL6, IGFBP3, HSD11B2, HMGA1, RNH1
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Rheumatoid Nodule
Wikipedia
The occurrence of nodules in the lung of miners exposed to silica dust was known as Caplan’s syndrome. [2] Rarely, the nodules occur at diverse sites on body (e.g. upper eyelid , distal region of the soles of the feet, vulva and internally in the gallbladder , lung, heart valves , larynx , and spine ). [3] Rheumatoid nodules can vary in size from 2 mm to 5 cm and are usually rather firm to the touch. ... External links [ edit ] Classification D ICD - 10 : M06.3 MeSH : D012218 v t e Diseases of joints General Arthritis Monoarthritis Oligoarthritis Polyarthritis Symptoms Joint pain Joint stiffness Inflammatory Infectious Septic arthritis Tuberculosis arthritis Crystal Chondrocalcinosis CPPD (Psudogout) Gout Seronegative Reactive arthritis Psoriatic arthritis Ankylosing spondylitis Other Juvenile idiopathic arthritis Rheumatoid arthritis Felty's syndrome Palindromic rheumatism Adult-onset Still's disease Noninflammatory Hemarthrosis Osteoarthritis Heberden's node Bouchard's nodes Osteophyte