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Suberosis
Wikipedia
Med Contemp 73,235-243 External links [ edit ] Classification D ICD - 10 : J67.3 ICD - 9-CM : 495.3 DiseasesDB : 29638 v t e Diseases of the respiratory system Upper RT (including URTIs , common cold ) Head sinuses Sinusitis nose Rhinitis Vasomotor rhinitis Atrophic rhinitis Hay fever Nasal polyp Rhinorrhea nasal septum Nasal septum deviation Nasal septum perforation Nasal septal hematoma tonsil Tonsillitis Adenoid hypertrophy Peritonsillar abscess Neck pharynx Pharyngitis Strep throat Laryngopharyngeal reflux (LPR) Retropharyngeal abscess larynx Croup Laryngomalacia Laryngeal cyst Laryngitis Laryngopharyngeal reflux (LPR) Laryngospasm vocal cords Laryngopharyngeal reflux (LPR) Vocal fold nodule Vocal fold paresis Vocal cord dysfunction epiglottis Epiglottitis trachea Tracheitis Laryngotracheal stenosis Lower RT / lung disease (including LRTIs ) Bronchial / obstructive acute Acute bronchitis chronic COPD Chronic bronchitis Acute exacerbation of COPD ) Asthma ( Status asthmaticus Aspirin-induced Exercise-induced Bronchiectasis Cystic fibrosis unspecified Bronchitis Bronchiolitis Bronchiolitis obliterans Diffuse panbronchiolitis Interstitial / restrictive ( fibrosis ) External agents/ occupational lung disease Pneumoconiosis Aluminosis Asbestosis Baritosis Bauxite fibrosis Berylliosis Caplan's syndrome Chalicosis Coalworker's pneumoconiosis Siderosis Silicosis Talcosis Byssinosis Hypersensitivity pneumonitis Bagassosis Bird fancier's lung Farmer's lung Lycoperdonosis Other ARDS Combined pulmonary fibrosis and emphysema Pulmonary edema Löffler's syndrome / Eosinophilic pneumonia Respiratory hypersensitivity Allergic bronchopulmonary aspergillosis Hamman-Rich syndrome Idiopathic pulmonary fibrosis Sarcoidosis Vaping-associated pulmonary injury Obstructive / Restrictive Pneumonia / pneumonitis By pathogen Viral Bacterial Pneumococcal Klebsiella Atypical bacterial Mycoplasma Legionnaires' disease Chlamydiae Fungal Pneumocystis Parasitic noninfectious Chemical / Mendelson's syndrome Aspiration / Lipid By vector/route Community-acquired Healthcare-associated Hospital-acquired By distribution Broncho- Lobar IIP UIP DIP BOOP-COP NSIP RB Other Atelectasis circulatory Pulmonary hypertension Pulmonary embolism Lung abscess Pleural cavity / mediastinum Pleural disease Pleuritis/pleurisy Pneumothorax / Hemopneumothorax Pleural effusion Hemothorax Hydrothorax Chylothorax Empyema/pyothorax Malignant Fibrothorax Mediastinal disease Mediastinitis Mediastinal emphysema Other/general Respiratory failure Influenza Common cold SARS Coronavirus disease 2019 Idiopathic pulmonary haemosiderosis Pulmonary alveolar proteinosis This article about a medical condition affecting the respiratory system is a stub .
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Opisthotonus
Wikipedia
A similar tonic posturing may be seen in Sandifer syndrome . Poisoning [ edit ] Opisthotonus can sometimes be seen in lithium intoxication. ... Opisthotonus is a symptom of " lavender foal syndrome ", a lethal genetic disorder in horses. [4] Sir Rudolph Peters, in Oxford, introduced thiamine -deprived pigeons as a model for understanding how thiamine deficiency can lead to the pathological-physiological symptoms of beriberi . ... Lay summary – New Scientist (23 November 2011). ^ "Lavender foal syndrome fact sheet" . James A. Baker Institute for Animal Health. ... External links [ edit ] Classification D ICD - 9-CM : 781.0 DiseasesDB : 31293 External resources MedlinePlus : 003195 v t e Symptoms and signs relating to movement and gait Gait Gait abnormality CNS Scissor gait Cerebellar ataxia Festinating gait Marche à petit pas Propulsive gait Stomping gait Spastic gait Magnetic gait Truncal ataxia Muscular Myopathic gait Trendelenburg gait Pigeon gait Steppage gait Antalgic gait Coordination Ataxia Cerebellar ataxia Dysmetria Dysdiadochokinesia Pronator drift Dyssynergia Sensory ataxia Asterixis Abnormal movement Athetosis Tremor Fasciculation Fibrillation Posturing Abnormal posturing Opisthotonus Spasm Trismus Cramp Tetany Myokymia Joint locking Paralysis Flaccid paralysis Spastic paraplegia Spastic diplegia Spastic paraplegia Syndromes Monoplegia Diplegia / Paraplegia Hemiplegia Triplegia Tetraplegia / Quadruplegia General causes Upper motor neuron lesion Lower motor neuron lesion Weakness Hemiparesis Other Rachitic rosary Hyperreflexia Clasp-knife response
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Space Adaptation Syndrome
Wikipedia
Find sources: "Space adaptation syndrome" – news · newspapers · books · scholar · JSTOR ( September 2009 ) ( Learn how and when to remove this template message ) NASA astronauts acclimating themselves to space adaptation syndrome in a KC-135 airplane that flies parabolic arcs to create short periods of weightlessness. [1] In about two thirds of the passengers, these flights produce nausea, [2] [3] giving the plane its nickname "vomit comet". Space adaptation syndrome ( SAS ) or space sickness is a condition experienced by as many as half of all space travelers during their adaptation to weightlessness once in orbit. [4] It is the opposite of terrestrial motion sickness since it occurs when the environment and the person appear visually to be in motion relative to one another even though there is no corresponding sensation of bodily movement originating from the vestibular system . [5] Contents 1 Cause and remedy 2 Impacts to worker safety 3 History 4 See also 5 References Cause and remedy [ edit ] Your body just isn't built to deal with zero-gravity. ... The limbic system may be the neural mismatch center of the brain." [7] At present a "fully adequate theory of motion sickness is not presently available" but at present the sensory conflict theory, referring to "a discontinuity between either visual, proprioceptive, and somatosensory input, or semicircular canal and otolith input", may be the best available. [8] Space adaptation syndrome or space sickness is a kind of motion sickness that can occur when one's surroundings visually appear to be in motion, but without a corresponding sense of bodily motion. ... Retrieved 2008-02-07 . v t e Consequences of external causes Temperature Elevated Hyperthermia Heat syncope Reduced Hypothermia Immersion foot syndromes Trench foot Tropical immersion foot Warm water immersion foot Chilblains Frostbite Aerosol burn Cold intolerance Acrocyanosis Erythrocyanosis crurum Radiation Radiation poisoning Radiation burn Chronic radiation keratosis Eosinophilic, polymorphic, and pruritic eruption associated with radiotherapy Radiation acne Radiation-induced cancer Radiation recall reaction Radiation-induced erythema multiforme Radiation-induced hypertrophic scar Radiation-induced keloid Radiation-induced morphea Air Hypoxia / Asphyxia Barotrauma Aerosinusitis Decompression sickness High altitude Altitude sickness Chronic mountain sickness Death zone HAPE HACE Food Starvation Maltreatment Physical abuse Sexual abuse Psychological abuse Travel Motion sickness Seasickness Airsickness Space adaptation syndrome Adverse effect Hypersensitivity Anaphylaxis Angioedema Allergy Arthus reaction Adverse drug reaction Other Electrical injury Drowning Lightning injuries Ungrouped skin conditions resulting from physical factors Dermatosis neglecta Pinch mark Pseudoverrucous papules and nodules Sclerosing lymphangitis Tropical anhidrotic asthenia UV-sensitive syndrome environmental skin conditions Electrical burn frictional/traumatic/sports Black heel and palm Equestrian perniosis Jogger's nipple Pulling boat hands Runner's rump Surfer's knots Tennis toe Vibration white finger Weathering nodule of ear Wrestler's ear Coral cut Painful fat herniation Uranium dermatosis iv use Skin pop scar Skin track Slap mark Pseudoacanthosis nigricans Narcotic dermopathy v t e Motion sickness Types Airsickness Seasickness Simulator sickness Ski sickness Space adaptation syndrome Virtual reality sickness Medicine treatment Bonine Cinnarizine Dramamine Marezine Promethazine Transdermscop Related Bárány chair Sickness bag v t e Space medicine Main areas Artificial gravity Astronautical hygiene Bioastronautics Neuroscience in space Space exposure Space food Space nursing Space weather Weightlessness Illness and injuries Asthenization Ebullism Illness and injuries during spaceflight Medical treatment during spaceflight Space adaptation syndrome Space and survival Spaceflight osteopenia Organizations Aerospace Medical Association National Space Biomedical Research Institute Rubicon Foundation Space Nursing Society Other topics Adverse health effects from lunar dust exposure Cardiac rhythm problems during space flight Central nervous system effects from radiation exposure during spaceflight Effect of spaceflight on the human body Effects of sleep deprivation in space Epidemiology data for low-linear energy transfer radiation Sleep in space Health threat from cosmic rays Intervertebral disc damage and spaceflight List of microorganisms tested in outer space Psychological and sociological effects of spaceflight Radiobiology evidence for protons and HZE nuclei Reduced muscle mass, strength and performance in space Renal stone formation in space Spaceflight radiation carcinogenesis Team composition and cohesion in spaceflight missions Visual impairment due to intracranial pressure v t e Spaceflight General Astrodynamics History Timeline Space Race Asian Space Race Records Accidents and incidents Space launch Space policy Australia China European Union India Japan Russia Soviet Union United States Space law Outer Space Treaty Rescue Agreement Space Liability Convention Registration Convention Moon Treaty Space warfare Space force Militarisation of space Private spaceflight Applications Astronomy Earth observation Archaeology Imagery and mapping Reconnaissance Weather and environment monitoring Communications satellite Internet Radio Telephone Television Satellite navigation Commercial use of space Space launch market competition Space architecture Space exploration Space research Space technology Space weather Human spaceflight General Astronaut commercial Life-support system Animals in space Bioastronautics Space suit Extravehicular activity Weightlessness Space toilet Space tourism Space colonization Space diving Programs Vostok Mercury Voskhod Gemini Soyuz Apollo Skylab Apollo–Soyuz Space Shuttle Mir Shuttle–Mir International Space Station Shenzhou Tiangong Artemis Health issues Effect of spaceflight on the human body Space adaptation syndrome Health threat from cosmic rays Space psychology Psychological and sociological effects Space and survival Space medicine Space nursing Spacecraft Launch vehicle Rocket Space capsule Orbital module Reentry capsule Service module Spaceplane Robotic spacecraft Satellite Space probe Lander Rover Self-replicating spacecraft Space telescope Spacecraft propulsion Rocket engine Electric propulsion Solar sail Gravity assist Destinations Sub-orbital Orbital Geocentric Geosynchronous Interplanetary Interstellar Intergalactic Space launch Direct ascent Escape velocity Expendable and reusable launch systems Launch pad Non-rocket spacelaunch Spaceport Ground segment Flight controller Ground station Pass Mission control center Space agencies CoNAE ASA ASA AEB CSA CNSA ESA CNES DLR ISRO LAPAN ISA ISA ASI AEM JAXA NADA KARI SUPARCO Roscosmos SNSA SSAU UKSA NASA / USSF Category Portal WikiProject
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Allergic Conjunctivitis
Wikipedia
External links [ edit ] Classification D ICD - 10 : H10.1 ICD - 9-CM : 372.14 MeSH : D003233 DiseasesDB : 30842 SNOMED CT : 473460002 External resources MedlinePlus : 001031 Allergic Conjunctivitis at the US National Library of Medicine Medical Subject Headings (MeSH) v t e Allergic conditions Respiratory system Allergic rhinitis (hay fever) Asthma Hypersensitivity pneumonitis Eosinophilic pneumonia Eosinophilic granulomatosis with polyangiitis Allergic bronchopulmonary aspergillosis Farmer's lung Laboratory animal allergy Skin Angioedema Urticaria Atopic dermatitis Allergic contact dermatitis Hypersensitivity vasculitis Blood and immune system Serum sickness Circulatory system Anaphylaxis Digestive system Coeliac disease Eosinophilic gastroenteritis Eosinophilic esophagitis Food allergy Egg allergy Milk intolerance Nervous system Eosinophilic meningitis Genitourinary system Acute interstitial nephritis Other conditions Drug allergy Allergic conjunctivitis Latex allergy v t e Diseases of the human eye Adnexa Eyelid Inflammation Stye Chalazion Blepharitis Entropion Ectropion Lagophthalmos Blepharochalasis Ptosis Blepharophimosis Xanthelasma Ankyloblepharon Eyelash Trichiasis Madarosis Lacrimal apparatus Dacryoadenitis Epiphora Dacryocystitis Xerophthalmia Orbit Exophthalmos Enophthalmos Orbital cellulitis Orbital lymphoma Periorbital cellulitis Conjunctiva Conjunctivitis allergic Pterygium Pseudopterygium Pinguecula Subconjunctival hemorrhage Globe Fibrous tunic Sclera Scleritis Episcleritis Cornea Keratitis herpetic acanthamoebic fungal Exposure Photokeratitis Corneal ulcer Thygeson's superficial punctate keratopathy Corneal dystrophy Fuchs' Meesmann Corneal ectasia Keratoconus Pellucid marginal degeneration Keratoglobus Terrien's marginal degeneration Post-LASIK ectasia Keratoconjunctivitis sicca Corneal opacity Corneal neovascularization Kayser–Fleischer ring Haab's striae Arcus senilis Band keratopathy Vascular tunic Iris Ciliary body Uveitis Intermediate uveitis Hyphema Rubeosis iridis Persistent pupillary membrane Iridodialysis Synechia Choroid Choroideremia Choroiditis Chorioretinitis Lens Cataract Congenital cataract Childhood cataract Aphakia Ectopia lentis Retina Retinitis Chorioretinitis Cytomegalovirus retinitis Retinal detachment Retinoschisis Ocular ischemic syndrome / Central retinal vein occlusion Central retinal artery occlusion Branch retinal artery occlusion Retinopathy diabetic hypertensive Purtscher's of prematurity Bietti's crystalline dystrophy Coats' disease Sickle cell Macular degeneration Retinitis pigmentosa Retinal haemorrhage Central serous retinopathy Macular edema Epiretinal membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary juvenile glaucoma Floater Leber's hereditary optic neuropathy Red eye Globe rupture Keratomycosis Phthisis bulbi Persistent fetal vasculature / Persistent hyperplastic primary vitreous Persistent tunica vasculosa lentis Familial exudative vitreoretinopathy Pathways Optic nerve Optic disc Optic neuritis optic papillitis Papilledema Foster Kennedy syndrome Optic atrophy Optic disc drusen Optic neuropathy Ischemic anterior (AION) posterior (PION) Kjer's Leber's hereditary Toxic and nutritional Strabismus Extraocular muscles Binocular vision Accommodation Paralytic strabismus Ophthalmoparesis Chronic progressive external ophthalmoplegia Kearns–Sayre syndrome palsies Oculomotor (III) Fourth-nerve (IV) Sixth-nerve (VI) Other strabismus Esotropia / Exotropia Hypertropia Heterophoria Esophoria Exophoria Cyclotropia Brown's syndrome Duane syndrome Other binocular Conjugate gaze palsy Convergence insufficiency Internuclear ophthalmoplegia One and a half syndrome Refraction Refractive error Hyperopia Myopia Astigmatism Anisometropia / Aniseikonia Presbyopia Vision disorders Blindness Amblyopia Leber's congenital amaurosis Diplopia Scotoma Color blindness Achromatopsia Dichromacy Monochromacy Nyctalopia Oguchi disease Blindness / Vision loss / Visual impairment Anopsia Hemianopsia binasal bitemporal homonymous Quadrantanopia subjective Asthenopia Hemeralopia Photophobia Scintillating scotoma Pupil Anisocoria Argyll Robertson pupil Marcus Gunn pupil Adie syndrome Miosis Mydriasis Cycloplegia Parinaud's syndrome Other Nystagmus Childhood blindness Infections Trachoma Onchocerciasis v t e Hypersensitivity and autoimmune diseases Type I / allergy / atopy ( IgE ) Foreign Atopic eczema Allergic urticaria Allergic rhinitis (Hay fever) Allergic asthma Anaphylaxis Food allergy common allergies include: Milk Egg Peanut Tree nut Seafood Soy Wheat Penicillin allergy Autoimmune Eosinophilic esophagitis Type II / ADCC IgM IgG Foreign Hemolytic disease of the newborn Autoimmune Cytotoxic Autoimmune hemolytic anemia Immune thrombocytopenic purpura Bullous pemphigoid Pemphigus vulgaris Rheumatic fever Goodpasture syndrome Guillain–Barré syndrome " Type V "/ receptor Graves' disease Myasthenia gravis Pernicious anemia Type III ( Immune complex ) Foreign Henoch–Schönlein purpura Hypersensitivity vasculitis Reactive arthritis Farmer's lung Post-streptococcal glomerulonephritis Serum sickness Arthus reaction Autoimmune Systemic lupus erythematosus Subacute bacterial endocarditis Rheumatoid arthritis Type IV / cell-mediated ( T cells ) Foreign Allergic contact dermatitis Mantoux test Autoimmune Diabetes mellitus type 1 Hashimoto's thyroiditis Multiple sclerosis Coeliac disease Giant-cell arteritis Postorgasmic illness syndrome Reactive arthritis GVHD Transfusion-associated graft versus host disease Unknown/ multiple Foreign Hypersensitivity pneumonitis Allergic bronchopulmonary aspergillosis Transplant rejection Latex allergy (I+IV) Autoimmune Sjögren syndrome Autoimmune hepatitis Autoimmune polyendocrine syndrome APS1 APS2 Autoimmune adrenalitis Systemic autoimmune disease
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Anal Fistula
Wikipedia
External links [ edit ] Classification D ICD - 10 : K60.3 ICD - 9-CM : 565.1 MeSH : D012003 External resources eMedicine : med/2710 Patient UK : Anal fistula Wikimedia Commons has media related to Anal fistula . v t e Diseases of the digestive system Upper GI tract Esophagus Esophagitis Candidal Eosinophilic Herpetiform Rupture Boerhaave syndrome Mallory–Weiss syndrome UES Zenker's diverticulum LES Barrett's esophagus Esophageal motility disorder Nutcracker esophagus Achalasia Diffuse esophageal spasm Gastroesophageal reflux disease (GERD) Laryngopharyngeal reflux (LPR) Esophageal stricture Megaesophagus Esophageal intramural pseudodiverticulosis Stomach Gastritis Atrophic Ménétrier's disease Gastroenteritis Peptic (gastric) ulcer Cushing ulcer Dieulafoy's lesion Dyspepsia Pyloric stenosis Achlorhydria Gastroparesis Gastroptosis Portal hypertensive gastropathy Gastric antral vascular ectasia Gastric dumping syndrome Gastric volvulus Buried bumper syndrome Gastrinoma Zollinger–Ellison syndrome Lower GI tract Enteropathy Small intestine ( Duodenum / Jejunum / Ileum ) Enteritis Duodenitis Jejunitis Ileitis Peptic (duodenal) ulcer Curling's ulcer Malabsorption : Coeliac Tropical sprue Blind loop syndrome Small bowel bacterial overgrowth syndrome Whipple's Short bowel syndrome Steatorrhea Milroy disease Bile acid malabsorption Large intestine ( Appendix / Colon ) Appendicitis Colitis Pseudomembranous Ulcerative Ischemic Microscopic Collagenous Lymphocytic Functional colonic disease IBS Intestinal pseudoobstruction / Ogilvie syndrome Megacolon / Toxic megacolon Diverticulitis / Diverticulosis / SCAD Large and/or small Enterocolitis Necrotizing Gastroenterocolitis IBD Crohn's disease Vascular : Abdominal angina Mesenteric ischemia Angiodysplasia Bowel obstruction : Ileus Intussusception Volvulus Fecal impaction Constipation Diarrhea Infectious Intestinal adhesions Rectum Proctitis Radiation proctitis Proctalgia fugax Rectal prolapse Anismus Anal canal Anal fissure / Anal fistula Anal abscess Hemorrhoid Anal dysplasia Pruritus ani GI bleeding Blood in stool Upper Hematemesis Melena Lower Hematochezia Accessory Liver Hepatitis Viral hepatitis Autoimmune hepatitis Alcoholic hepatitis Cirrhosis PBC Fatty liver NASH Vascular Budd–Chiari syndrome Hepatic veno-occlusive disease Portal hypertension Nutmeg liver Alcoholic liver disease Liver failure Hepatic encephalopathy Acute liver failure Liver abscess Pyogenic Amoebic Hepatorenal syndrome Peliosis hepatis Metabolic disorders Wilson's disease Hemochromatosis Gallbladder Cholecystitis Gallstone / Cholelithiasis Cholesterolosis Adenomyomatosis Postcholecystectomy syndrome Porcelain gallbladder Bile duct / Other biliary tree Cholangitis Primary sclerosing cholangitis Secondary sclerosing cholangitis Ascending Cholestasis / Mirizzi's syndrome Biliary fistula Haemobilia Common bile duct Choledocholithiasis Biliary dyskinesia Sphincter of Oddi dysfunction Pancreatic Pancreatitis Acute Chronic Hereditary Pancreatic abscess Pancreatic pseudocyst Exocrine pancreatic insufficiency Pancreatic fistula Other Hernia Diaphragmatic Congenital Hiatus Inguinal Indirect Direct Umbilical Femoral Obturator Spigelian Lumbar Petit's Grynfeltt-Lesshaft Undefined location Incisional Internal hernia Richter's Peritoneal Peritonitis Spontaneous bacterial peritonitis Hemoperitoneum Pneumoperitoneum Authority control BNE : XX4769476 BNF : cb12550274f (data) LCCN : sh85048893 SUDOC : 034785264
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Radiculopathy
Wikipedia
It may be secondary to intervertebral disk herniation (most commonly at C7 and then the C6 level), degenerative disc disease , osteoarthritis , facet joint degeneration/hypertrophy, ligamentous hypertrophy , spondylolisthesis , or a combination of these factors. [3] [4] Other possible causes of radiculopathy include neoplastic disease , infections such as shingles , HIV , or Lyme disease , spinal epidural abscess , spinal epidural hematoma , proximal diabetic neuropathy , Tarlov cysts , or, more rarely, sarcoidosis , arachnoiditis , tethered spinal cord syndrome , or transverse myelitis . [3] [ verification needed ] Repeated, longer term exposure (5 years or more) to certain work-related activities may put people at risk of developing lumbosacral radiculopathy. [5] These behaviours may include physically demanding work, bending over or twisting at the trunk, lifting and carrying, or a combination of these activities. [5] Less common causes of radiculopathy include injury caused by tumor (which can compress nerve roots locally) and diabetes (which can effectively cause ischemia or lack of blood flow to nerves). [ medical citation needed ] Diagnosis [ edit ] Projectional radiograph of a man presenting with pain by the nape and left shoulder, showing a stenosis of the left intervertebral foramen of cervical spinal nerve 4 , corresponding with the affected dermatome . ... Lyme radiculopathy is usually worse at night and accompanied by extreme sleep disturbance, lymphocytic meningitis with variable headache and no fever, and sometimes by facial palsy or Lyme carditis . [12] Lyme can also cause a milder, chronic radiculopathy an average of 8 months after the acute illness. [3] Lyme can be confirmed by blood antibody tests and possibly lumbar puncture . [9] [3] If present, the above conditions should be treated immediately. [3] Although most cases of radiculopathy are compressive and resolve with conservative treatment within 4–6 weeks, guidelines for managing radiculopathy recommend first excluding possible causes that, although rare, require immediate attention, among them the following. Cauda equina syndrome should be investigated in case of saddle anesthesia , loss of bladder or bowel control, or leg weakness. [3] Cancer should be suspected if there is previous history of cancer, unexplained weight loss, or low-back pain that does not decrease by lying down or is unremitting. [3] Spinal epidural abscess is more common among those with diabetes mellitus or immunocompromised , who use intravenous drugs , or had spinal surgery , injection or catheter ; it typically causes fever , leukocytosis and increased erythrocyte sedimentation rate . [3] If any of the previous is suspected, urgent magnetic resonance imaging is recommended for confirmation. [3] Proximal diabetic neuropathy typically affects middle aged and older people with well-controlled type-2 diabetes mellitus ; onset is sudden causing pain usually in multiple dermatomes quickly followed by weakness. [ citation needed ] Investigations If symptoms do not improve after 4–6 weeks of conservative treatment, or the person is more than 50 years old, further tests are recommended. [3] The American College of Radiology recommends that projectional radiography is the most appropriate initial study in all patients with chronic neck pain. [13] Two additional diagnostic tests that may be of use are magnetic resonance imaging and electrodiagnostic testing. ... "Work-relatedness of lumbosacral radiculopathy syndrome: Review and dose-response meta-analysis" . ... "Course and Outcome of Early European Lyme Neuroborreliosis (Bannwarth Syndrome): Clinical and Laboratory Findings" . ... External links [ edit ] Classification D ICD - 10 : G54, M54.1 ICD - 9-CM : 723.4 , 724.4 , 729.2 MeSH : D011843 DiseasesDB : 29522 SNOMED CT : 72274001 Radiculopathy at the US National Library of Medicine Medical Subject Headings (MeSH) v t e Spinal disease Deforming Spinal curvature Kyphosis Lordosis Scoliosis Other Scheuermann's disease Torticollis Spondylopathy inflammatory Spondylitis Ankylosing spondylitis Sacroiliitis Discitis Spondylodiscitis Pott disease non inflammatory Spondylosis Spondylolysis Spondylolisthesis Retrolisthesis Spinal stenosis Facet syndrome Back pain Neck pain Upper back pain Low back pain Coccydynia Sciatica Radiculopathy Intervertebral disc disorder Schmorl's nodes Degenerative disc disease Spinal disc herniation Facet joint arthrosis v t e Diseases relating to the peripheral nervous system Mononeuropathy Arm median nerve Carpal tunnel syndrome Ape hand deformity ulnar nerve Ulnar nerve entrapment Froment's sign Ulnar tunnel syndrome Ulnar claw radial nerve Radial neuropathy Wrist drop Cheiralgia paresthetica long thoracic nerve Winged scapula Backpack palsy Leg lateral cutaneous nerve of thigh Meralgia paraesthetica tibial nerve Tarsal tunnel syndrome plantar nerve Morton's neuroma superior gluteal nerve Trendelenburg's sign sciatic nerve Piriformis syndrome Cranial nerves See Template:Cranial nerve disease Polyneuropathy and Polyradiculoneuropathy HMSN Charcot–Marie–Tooth disease Dejerine–Sottas disease Refsum's disease Hereditary spastic paraplegia Hereditary neuropathy with liability to pressure palsy Familial amyloid neuropathy Autoimmune and demyelinating disease Guillain–Barré syndrome Chronic inflammatory demyelinating polyneuropathy Radiculopathy and plexopathy Brachial plexus injury Thoracic outlet syndrome Phantom limb Other Alcoholic polyneuropathy Other General Complex regional pain syndrome Mononeuritis multiplex Peripheral neuropathy Neuralgia Nerve compression syndrome
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Muscular Dystrophy, Congenital, Producing Arthrogryposis
Omim
Clinical Features Pearson and Fowler (1963) described nonprogressive myopathy in sibs, producing the arthrogryposis syndrome. A similar situation may have existed in the family reported by Banker et al. (1957). ... The 380-gm male fetus had multiple contractures and the same histologic changes in skeletal muscle. Joints - Arthrogryposis syndrome - Multiple fetal contractures Muscle - Myopathy Misc - Absent fetal movement Lab - Skeletal muscle replaced by adipose connective tissue Inheritance - Autosomal recessive ▲ Close
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Humeroradial Synostosis With Craniofacial Anomalies
Omim
Al-Hassnan and Teebi (2007) reported 2 sisters, born of consanguineous Saudi parents, who had a syndromic form of humeroradial synostosis. ... After an extensive review of the literature, Al-Hassnan and Teebi (2007) concluded that their cases represent a previously unrecognized syndromic disorder. HEENT - Plagiobrachycephaly - Prominent forehead - Broad nasal root - Small ears - Hypoplastic earlobes Inheritance - Autosomal recessive Skel - Multiple synostosis - Humeroradial synostosis - Carpal synostosis - Tarsal synostosis - Phalangeal synostosis - Agenesis of distal phalanges of postaxial digits ▲ Close
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Acetaminophen Metabolism
Omim
Evidence was presented by de Morais et al. (1989) that, in comparison with normal subjects, glucuronidation of acetaminophen is impaired in subjects with Gilbert syndrome (143500), a disorder in which glucuronidation of bilirubin is impaired. ... Inheritance - Autosomal dominant Lab - Impaired acetaminophen glucuronidation in Gilbert syndrome (143500) Skin - Jaundice ▲ Close
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Ophthalmoplegic Neuromuscular Disorder With Abnormal Mitochondria
Omim
Okamoto et al. (1981) described the ophthalmoplegia-plus syndrome in brother and sister. Computerized tomography scan showed diffuse, low-density deep cerebral white material. ... The disorder described by Tamura et al. (1974) has similarities to the Kearns-Sayre syndrome (530000), appears to represent a mitochondrial cytopathy, and may be mitochondrially inherited.
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Episodic Muscle Weakness, X-Linked
Omim
Clinical Features Ryan et al. (1999) reported a family with clinical and pathologic features of a novel syndrome of episodic muscle weakness. Eight males in generations 2 and 4 demonstrated the features of the disorder, consistent with X-linked inheritance. ... The clinical phenotype had features suggestive both of the congenital myasthenic syndromes (see 254210) and of ion-channel disorders such as periodic paralyses (see 170400).
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Adrenal Cancer
Gard
However, certain genetic conditions such as multiple endocrine neoplasia type 2 , Li-Fraumeni syndrome , Von Hippel-Lindau syndrome , neurofibromatosis type I , and Carney complex are associated with an increased risk of developing adrenal tumors and cancer.
- Aneurysm, Intracranial Berry, 2 Omim
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Polyembryoma
Wikipedia
It has been found in association with Klinefelter syndrome . [1] References [ edit ] ^ Beresford L, Fernandez CV, Cummings E, Sanderson S, Ming-Yu W, Giacomantonio M (2003). "Mediastinal polyembryoma associated with Klinefelter syndrome". J. Pediatr. Hematol. Oncol . 25 (4): 321–3. doi : 10.1097/00043426-200304000-00011 .
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3-Hydroxyacyl-Coa Dehydrogenase Deficiency
Medlineplus
This condition may explain some cases of sudden infant death syndrome (SIDS), which is defined as unexplained death in babies younger than 1 year. ... This disorder is sometimes mistaken for Reye syndrome, a severe disorder that may develop in children while they appear to be recovering from viral infections such as chicken pox or flu. Most cases of Reye syndrome are associated with the use of aspirin during these viral infections.
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Hhhh Syndrome
Omim
Clinical Features Haar and Dyken (1977) described a family with many affected members in a pattern consistent with X-linked recessive inheritance with variable expression in heterozygous females. The disorder consisted of congenital left hemiparesis with subsequent development of left hemihypoplasia and athetoid posturing of the left hand. They referred to an unpublished family in which a young male proband, his brother, his sister and a maternal uncle were born with right hemiparesis with subsequent development of hemiatrophy, involuntary movements, and seizures. The authors labeled the disorder autosomal dominant, but X-linked inheritance seems equally or more likely. An instance of parental consanguinity in the family raises a question also of autosomal recessive inheritance.
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Autism, Susceptibility To, X-Linked 3
Omim
'Autism spectrum disorder,' sometimes referred to as ASD, is a broader phenotype encompassing the less severe disorders Asperger syndrome (see ASPG1; 608638) and pervasive developmental disorder, not otherwise specified (PDD-NOS). ... Mental retardation coexists in approximately two-thirds of individuals with ASD, except for Asperger syndrome, in which mental retardation is conspicuously absent (Jones et al., 2008). ... INHERITANCE - X-linked NEUROLOGIC Central Nervous System - Impaired social interaction - Impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures - Lack of peer relationships - Impaired language development - Lack of spontaneous play - Restrictive behavior, interests, and activities - Stereotyped, repetitive behavior - Inflexible adherence to routines or rituals - Mental retardation in 75% - Seizures in 15-30% - EEG abnormalities in 20-50% LABORATORY ABNORMALITIES - Increased serum serotonin in 25% MISCELLANEOUS - Onset by 3 years of age - Male to female ratio 4:1 - Occurs in 2-5 per 10,000 individuals - Genetic heterogeneity (see 209850 ) - Associated with tuberous sclerosis ( 191100 ) - Associated with untreated phenylketonuria ( 261600 ) - Genetic heterogeneity (see 209850 ) - Allelic disorder to Rett syndrome ( 312750 ) MOLECULAR BASIS - Susceptibility conferred by mutation in the methyl-CpG binding protein-2 gene (MECP2, 300005.0011 ) ▲ Close
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Achalasia, Familial Esophageal
Omim
Koivukangas et al. (1973) found Sjogren syndrome and achalasia in 2 sisters. (The Sjogren syndrome present in this family consisted of the triad of keratoconjunctivitis sicca, xerostomia, and rheumatoid arthritis or other connective tissue disease.) ... These brothers may have had the syndrome of glucocorticoid deficiency and achalasia (231550) because in the 8-year-old 'the clinical picture was obscured by the fact that the patient was hyperpigmented and had low plasma steroids.'NOS1, HLA-DQA1, HLA-DQB1, CRLF1, SPRY2, LMNA, AAAS, GUCY1A1, IARS2, ACTB, TRAPPC11, GMPPA, GLA, FLVCR1, NPNT, FUT3, POMC, KIT, PTPN22, RBM45, WNT2, HLA-DRB1, TP53, TNF, RET, IL22, ECI1, IL23A, IL10, DBI, TWNK, ISLR2, CCK, CALR, PNMA2, MMP2, IL13, MMP9, VIPR1, S100B, S100A1, RNASE2, AGA, POLG, SERPINB2, SERPINE1, NOS3, LTA, MIR130A
- Keloid Formation Omim
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Hereditary Clear Cell Renal Cell Carcinoma
Orphanet
Hereditary clear cell renal cell carcinoma (ccRCC) is a hereditary renal cancer syndrome defined as development of ccRCC in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other tumor predisposing syndromes associated with ccRCC, such as tuberous sclerosis or Birt-Hogg-Dubbé syndrome.FLCN, VHL, HNF1A, SETD2, PBRM1, OGG1, BAP1, MTOR, KDM5C, MET, TSC1, HNF1B, GSTM1, PIK3CA, ERBB2, TFE3, GJB1, EPAS1, ALK, TP53, MITF, TSC2, IL6, ADIPOQ, KDR, PTGS2, PTEN, GSTT1, TGM2, GSTP1, ELOC, TNFSF10, PRCC, SLC2A1, MAPK8, FLT1, DAPK1, KDM6A, IL13, BIRC7, ARID1A, KRT7, APAF1, PVALB, ATM, POMC, APRT, SFRP2, L1CAM, HSPB1, ANXA4, KEAP1, RELA, IL4R, TEK, TMEM127, KRT8, RNF139, BIRC5, ALOX5, ALDH1A1, FLT4, SOD2, PAK1, UNC5C, NF2, SCARB1, DCLK3, IFNA2, NDRG1, PEBP1, HSPD1, CASP2, MUC4, CRABP1, PGK1, BTG3, SLC49A4, PRAME, CPQ, HSPA9, ZNF765, CUL7, WNK3, NAV3, CDK15, IL6R, CARD11, ZNF536, SHANK1, KCNMA1, LRP1B, CAPG, AHNAK, MYO3A, KRT32, CRYAB, INPP4B, MERTK, CSMD3, FAM111B, PDXDC1, PNKD, PIDD1, LMAN2L, LRRK2, ERN1, FPGT, CNN2, YIPF3, CTSB, SYNE2, ASB15, DNHD1, GRB7, CTSD, MSGN1, FAAH2, CILK1, TET2, AP5M1, AKAP13, RIOK2, FMN2, HARS1, EEF2, ZNF804A, NLRP12, OR4C13, VMO1, SPTBN4, RPL14, LDHB, BMPR1A, MLLT10, M6PR, SLC5A3, ALOX12B, ACY1, BRD3, ALAD, RYR1, PDHB, ROR1, ACHE, BCHE, TAGLN2, CRADD, CHEK2, NOD2, MALAT1, CCND1, MME, PDCD1, MDM2, VDR, HIF1A, HNF1A-AS1, AXL, CRP, HLA-G, VEGFA, RASSF1, MMP9, FH, MMP2, STAT3, MYC, CD274, SMUG1, TGFA, MPRIP, TBC1D9, TGFB1, AR, MIR200C, TNF, SMIM4, PCNA, BCL2, CDKN2A, AKT1, FOLH1, VIM, MIR21, PIK3CB, PIK3CD, IL10, MIR155, MIR210, CTLA4, SDHB, TFEB, CTNNB1, EPO, CASP3, EGFR, EGF, CA9, IL4, PIK3CG, CXCR4, IFNG, IFNA13, EZH2, ABCB1, LARP6, CD44, MIR126, IL2, IFNA1, IGF1, MIR204, PTHLH, TERT, PAX8, FN1, ELAVL2, MIR141, MIR30A, FHIT, CSF2, ESR1, MIR34A, XRCC1, PRKN, PAX2, ESR2, MUL1, NOTCH1, HAVCR1, DNMT1, CCK, MIR429, KIT, CASP8, COX2, CXCL8, MIR10B, DKK3, ABCG2, MIR221, HPGDS, MIR145, COL18A1, PDCD1LG2, CCL2, CXCL12, JAK2, MIR206, MIR205, NDRG2, MAPK1, PROM1, MTCO2P12, IL1B, SFRP1, HOTAIR, ALB, NFE2L2, MIR451A, SPP1, SLCO6A1, TGFBI, GSK3B, HGF, CBLL2, GSTK1, YAP1, HLA-A, SPOP, PVT1, NFKB1, KRAS, IGF1R, SPHK1, E2F1, MAPK3, ZEB2, ROCK1, AMACR, MCL1, EIF4EBP1, SMARCA1, PPARG, FOXM1, EPHA3, PECAM1, SMAD4, TIMP1, PKM, TIMP2, SLC16A4, SLC16A3, HNF4A, MMP1, SARDH, H3P10, CAV1, CDH1, CLU, PARP1, ACTB, CD38, MIR122, CDKN1A, MIR106B, HAVCR2, CD70, BSG, MLH1, MIR30C2, MIR200A, LDHA, MST1, LILRB1, HMGB1, CIB1, EPHB2, TWIST1, HSPA5, MTHFR, FOXO1, TUG1, LEP, MIR224, TCHP, SMAD2, HMGA2, LOXL2, FOXP3, MIR378A, EIF4E, MUC1, FAS, ITPR2, BRD4, PRKCA, IL18, DAB2IP, GABPA, PLIN2, SDHA, MIR183, SDHD, TMED7-TICAM2, PDGFRB, SERPINE1, CDKN1B, SOX2, YBX1, SOX4, CXCR2, TMED7, BHD, ACKR3, TICAM2, IGFBP3, RUNX3, MIR15A, MIR144, RBX1, ASPSCR1, CD34, NEAT1, GNAS, KDM6B, DKK1, HEPACAM, HDAC1, SDS, CDK4, CDH6, IFNB1, HLA-C, DCTN6, ITGA5, SPINT2, ZNRD2, CDK1, IFI27, KHDRBS1, LEPR, MIR182, NNMT, MIR338, MT1G, TGFBR1, XIAP, APEH, TAP1, NEDD9, AURKA, MIR497, SORD, SOCS3, SMARCB1, SDHC, MICA, S100A9, PPARA, PRKAA1, PRKAB1, MAP2K1, H3P23, THRB, MSH2, TIMP3, MMP3, KISS1, MBD2, SQSTM1, MIR195, CA12, KRT19, GATA3, LGALS3, MIR203A, BRCA1, MIR22, MIR222, WT1, MCAM, EZR, MIR27A, B2M, MIR29A, MIR30C1, MYOF, PSMD9, RAB25, GAS5, CYP1A1, ZC3H12A, EDN1, EDNRB, SLC12A9, XRCC6, CYP1B1, KLF6, DEFB1, FABP7, MAP1LC3B, ACE, ANGPTL4, EN2, EPOR, HILPDA, SNAI2, ICAM1, SLC22A2, TCF4, ERBB4, MIR590, BMP6, MEG3, PGF, UCA1, CXCR1, CD24, ADIPOR1, CIP2A, ENG, BNIP3, KLK3, MIR125A, MAGEA6, SMYD2, TCF21, PDK1, VTCN1, MIR106A, ARHGAP24, TCF7L2, DUXAP8, FGF2, HDAC9, RBM10, CD80, MIR223, PCDH8, PFN1, FGFR3, ILK, BRAF, FABP5, CAPNS1, ANGPT1, ANGPT2, FBXW7, MIR185, APLN, LGALS1, NME1, SST, BECN1, EGLN1, MIR199B, MIR19A, JADE1, STK11, TESC, MIR200B, TNFRSF10B, EWSR1, CCN3, CD82, SNAI1, L2HGDH, CUL2, MIR17, LCN2, CAV2, CXCL10, ALPP, NUCB2, ROR2, MIR508, DCTN4, MIB1, CBFA2T2, ITGB1, GDE1, MIR181A2, LATS1, MED15, SART1, CASR, CD68, ABCC1, CD74, CDCP1, CMTM4, PRKAA2, REN, MKI67, TGFB2, KLF8, PPBP, CDKN2B, GSTM2, CISH, MIR29C, POU2F2, GTF2H1, SFPQ, FAM107A, FSTL1, TYMS, S100A1, WNK1, GPT, PMS2, MIR99A, LAT, PTBP1, UCN3, ABCC2, CMAS, PTK2, TLR1, NUP62, ACSS2, TPM1, MT1E, ASS1, BBC3, SIRT1, MOK, BRK1, TGFBR2, GATA5, TRPM3, CASC2, ESM1, VEGFC, MIR384, LUCAT1, SIX2, MAP3K8, HOTTIP, POSTN, MIR425, ADM, MTDH, HMOX1, ATG7, UHRF1, CTSK, NDUFA4L2, TFAP2A, FOXO3, LINC01194, CLDN7, PLAU, GOLPH3, SCD, HLA-DRB1, UCP1, EGLN3, MFAP1, CDK2, MIR29B2, RALBP1, COL11A2, PLK1, MIR29B1, SATB1, VCAM1, VCL, MIR373, ADAM17, ELOB, THBS1, TFRC, RETN, MIR452, TAZ, SYT1, RNF20, MAP3K7, ZEB1, TRBV20OR9-2, TGFBR3, GRHL2, TAP2, MIR372, MIR363, WLS, MUC13, ESRP2, CYTOR, STK3, GORASP1, RPL17, RPS6, RPL17-C18orf32, RBM14-RBM4, S100A4, S100A6, S100A8, S100A10, RAB4B-EGLN2, S100A11, S100B, CCL18, CCL21, SAV1, CXCL16, SELE, BCL2L2-PABPN1, RNASE3, MIR489, LOC110013312, FSD1, H3P8, LNCRNA-ATB, PTPRG, BHLHE41, LNCARSR, LOC110806263, GHET1, HMGN5, PANDAR, RAC1, RAF1, REG1A, FRTS1, COMETT, MARCKSL1, MUC3B, MIR1233-1, SET, SPAG4, SMN1, MIR486-1, SMN2, SNCA, FSCN1, MIR509-1, SOX9, SPARC, KLLN, TP73-AS1, SREBF1, ST14, MIR499A, STAT1, MIR490, STC1, KLHL1, MIR411, SLPI, SLC16A1, SYCE1L, MIR543, MIR877, SFRP4, SH3BP2, ST3GAL4, VTRNA2-1, SLC5A2, TEC, MIR663A, MIR630, SLC6A3, SLC12A3, MIR625, SLC15A1, CRNDE, MIR212, SLC50A1, CXCR6, MCRS1, KMT5A, HOXB13, SPTLC1, CXCL13, SLC34A2, TXNIP, CRB3, MCTS1, DLEC1, NES, FNIP1, MTHFD2, CCL27, HPSE, PGRMC1, EGLN2, LAMTOR2, RBM14, MIRLET7D, TFCP2L1, DLC1, AKT3, PTPRU, NOX4, G3BP1, PSME3, OBP2A, WNT3A, MIR10A, COL23A1, TRIM13, MIR100, SENP1, FLOT1, CDK2AP2, PAK4, AKR1A1, IRF9, PPARGC1A, MCAT, SUB1, EPB41L3, KANK1, ARC, SATB2, PPP1R13B, SIRT3, CACYBP, MUC17, SEC14L2, PACRG, OSR1, SNHG1, PSMB9, PLA2G15, QPCT, RWDD3, ATRNL1, INTS1, DKK4, PRRT2, ANGPTL3, NCOA6, FERMT2, PDLIM3, PCDH17, RPP14, HHLA2, MAGEA2B, WIF1, CADM2, PDCD4, SLC39A1, AGO2, SKA1, RASSF6, VASH1, SLFN5, DKK2, SMG1, SCO2, SPATA2, MIR337, FSD1L, MIR217, MIR216A, MIR215, SLC7A5, TCL6, MIR211, KDM5D, SOX7, RGS5, MIR130B, PPM1D, BHLHE40, KAT8, EIF3D, NAT10, CEP55, RIPK1, TRPM7, LAP, CD276, HIF1AN, WNT10A, MIR335, MIR133B, TOP2A, MIR96, MIR31, TP73, TPM3, KDM3A, NR2C2, TRPC6, MIR30B, UCHL1, ASRGL1, MIR28, PPP1R2C, MIR23B, MIR23A, MIR20A, TNFRSF10A, MIR19B1, PTTG1, KLF4, SLIT2, KL, QKI, ING4, AIM2, GAL3ST1, PCLAF, APH1A, MAML1, MIR150, MIR149, MIR146A, SNHG12, MIR143, MIR142, MIR137, PIWIL1, MAGI1, NRP2, FTO, NRP1, ACCS, RIOX2, MIR193A, CFLAR, MIR191, NR1I2, DLL4, NUDCD1, MIR184, MPC1, HSPB3, SF3B6, SPAG9, CLDN8, EBAG9, DCLK1, AURKB, BTG2, PSMB8, CD40, CD47, CD151, CDC20, CDH3, MAGEA2, SMAD3, EPCAM, LRPAP1, CDH15, LOX, CDK6, CDK7, LHX1, CEBPB, LDLR, CHI3L1, LAMA4, LAG3, KIF22, CMA1, CCR4, KLK1, ITGA7, COL5A1, COX8A, CREB1, CRH, CD40LG, MDM4, ANXA2, CCNB1, ANXA5, APC, NPTX2, APEX1, APOE, NONO, FASLG, NFKB2, MYCN, ATHS, ATP1A1, ATP1B1, MUC3A, BAX, BCL2L2, MRC1, BMP2, BST2, C1QBP, MIP, DDR1, CXCL9, CALR, CASP9, MGMT, RUNX1, MAP3K5, CRHBP, IL16, IL13RA2, IL11, EEF1A1, EGR1, EPHA2, CXCR3, GOT2, ENO1, ENO2, GLS, EP300, ERCC2, GC, ETFA, ETS1, GAS6, GAD1, G6PD, G6PC, F2R, F2RL1, FOS, F3, F12, PTK2B, FGFR2, FCGR3B, FCGR3A, FBN2, GRP, EDNRA, GSTM3, HSPA4, IL2RA, IL1A, IKBKB, CCN1, IGFBP7, CSF1R, IFNAR2, VCAN, CST3, IRF8, CYP2D6, HSPB2, HSPA2, TYMP, HSPA1B, HSPA1A, DAG1, NQO1, HOXA6, DIO1, DKC1, HNRNPA2B1, NR4A1, HK2, DUSP9, E2F3, P2RY1, FBP1, AGT, AGER, POU5F1, ENPP2, ALOX15, PDPK1, MAPK7, POLR2A, PPIA, PLG, ACVRL1, ALOX12, JAG1, ADAM10, MAP2K7, PIK3R1, SLC25A3, ADRA1A, PDZK1, PIM1, AHR, PRKCB, PML, DES, GNPTAB, LINC01234, CDC73, SLC52A2, DFFA, DNASE1L3, OTUD6B-AS1, ADIPOR2, DDC, NANOG, ADORA1, ADH7, DACH1, MIR3133, MIR1260B, DHDDS, LINC01094, LPCAT1, RASL11B, AGMAT, ZNF419, RIOX1, SAP30L, RTL10, DCN, NDNF, DNMT3A, DPP4, ZSCAN18, LGR6, COP1, ERAP2, MELTF-AS1, DVL2, FKBP10, E2F2, ADAMTS9-AS2, SCPEP1, MFSD14A, ACE2, HIVEP3, LY6G6D, ECE1, CTDSP1, NFE4, ADAM8, HIF3A, DSG2, OCLN, MRPL41, DNMT3B, FTX, DRD1, THORLNC, DRD2, ATN1, ACD, CENPH, COPS7B, RCAN1, USP46, DDX31, TNS3, GIHCG, ATPAF1, SMURF2, CYP27B1, PDGFD, CYP24A1, KISS1R, HAPLN1, CRYBA4, C19orf48, PYROXD2, AFAP1-AS1, CRYGD, SPZ1, NT5C1A, DOT1L, MAP1LC3A, MAK16, LINC00887, FILNC1, SNORD35B, ADRA2B, ACSS1, ORAI1, CRK, CORO6, CRHR2, CPOX, CRABP2, IGFN1, IL33, MED30, EGOT, LMLN, ATF2, SSH2, SNORD14E, SNORD14D, SNORD14C, SNORD14B, DNM1P35, UBASH3B, TRAP, CRYZ, CYP4B1, CTNNA1, TRIM8, TXNDC5, MIR1291, SLC35G2, MIR1236, CTAG1B, CCN2, CXXC4, AKT1S1, CXADR, HES4, FBXO11, RNF34, CYLD, MIR1290, CYP3A5, CSNK2A1, VMP1, SH3BGRL3, CSNK1E, RPAIN, MAPK14, SETD3, MINDY4, NLRC5, CSF1, MAGT1, TMPRSS13, CCDC8, MIR1294, SETDB2, SLC25A18, SESN2, CSF3, RASSF5, HAMP, AMFR, TRIB3, PPP1R12C, LINC01885, ANKHD1, EZH1, ASIC2, ERCC6L, F2, RNF111, XAF1, CMTM6, TMED9, UGT1A1, LNCSRLR, ACAT1, DDIT4, KRT20, GFOD1, CASZ1, SARS2, TREM2, TPTEP2-CSNK1E, LAPTM4B, ESRRA, RNF121, ESRRB, IMP3, PACC1, ESRRG, SNHG14, RNF125, TMEM45A, OXR1, ETS2, IRAIN, ETV1, PINX1, SDHAF2, SOX18, F2RL2, ECHS1, LEF1, SLC22A17, TLR7, CLEC1B, NUSAP1, AADAC, HSPA14, HAO2, FBLN1, TNFRSF12A, EGFL7, SDF4, FBN1, CHCHD2, SERPINA3, H3P42, H3P47, PLAC8, COMMD10, ACADM, NUB1, CDHR5, IL20RB, MNS16A, IL17D, RSF1, WWOX, RAB23, ACACA, SFMBT1, FABP1, TRIM33, ACSL1, ABL2, IL23A, SIRT6, HIKESHI, HJURP, ERG, ERCC4, CIAPIN1, ZMIZ1, SMURF1, RTN4, MAN1C1, CHMP1B, EFNA1, TIGAR, ADAMTS9, ADA, ACTG2, CHPT1, PRDM9, FAM20C, EIF4B, PNO1, ACTG1, SLC39A10, CEMIP, SAGE1, ARRDC3, ECT2, EP400, S1PR1, CP, ZNF492, ERV3-2, FNIP2, SEMA6A, DANCR, TRIM52-AS1, MTA3, LOC100507703, PHC1, SCYL1, RAB22A, CLTRN, ELANE, ELF5, ELK1, DOK4, IATPR, PAG1, EPHA1, EPHA5, CCAR1, EPHB4, ASF1B, ERBB3, ELN, NLRP2, ACLY, PNRC2, SMPD4, SUPT20H, RBM38, KCNQ1DN, GABRQ, NPTN-IT1, ZNF395, ENPEP, PANX2, TWNK, DIABLO, SPRY4-IT1, PPAN, METTL3, TRPV5, PARD3, MARK2, SUSD2, PDGFC, MYDGF, ACTA2, SULF2, ACR, EGFR-AS1, COX5B, WDR20, MIR196A2, C5AR1, VPS51, CA4, CA8, MIR199A2, MIR199A1, MIR198, MIR196A1, KLF5, MIR556, MIR572, CALCR, MIR192, MIR584, MIR186, CAPN1, ALDOB, PPAN-P2RY11, CASP10, CXCR5, CXADRP1, OPN1SW, BDNF, BGLAP, CEACAM1, MIR539, BIK, BNC1, BRS3, BMI1, BMP1, LINC00488, BMP4, BMP7, BMPR1B, BMX, CAPN2, MIR588, TIMD4, ENTPD1, CD19, MIR129-2, MS4A1, CD27, MIR124-3, CD28, CD36, MIR107, MIR134, MIR622, ALDH9A1, MIRLET7I, MIRLET7F2, MIRLET7C, MIRLET7B, ALDH3B1, MIR132, MIR136, CAT, CBS, RUNX2, MIR15B, RUNX1T1, MIR154, CBL, SERPINH1, MIR148A, ALDOA, CD14, MIR599, CCNC, CCNE1, CCT, MIR613, CD1D, MIR138-1, BCL2A1, BBS2, MIR24-1, MIR381, H4C15, POU5F1P3, DUXAP9, SMIM5, APOH, AQP1, MIR383, H3P16, APLP2, AQP4, MIR377, MIR376A1, MIR375, AQP9, ARG1, MIR367, MIR362, MIR20B, MIR24-2, MIR510, MIR502, MIR501, ANXA1, MIR498, AMBP, MIR193B, MIR495, MIR492, SNHG6, MIR146B, ALPI, ANXA6, MIR488, MIR409, MIR455, POTEM, ARG2, RHOB, ARHGDIB, ATP5F1A, MIR32, LINC00461, MIR30E, MIR30D, ATIC, IGFL2-AS1, ATP2B1, ATP5MC1, MIR328, POU5F1P4, ATP5MC2, MIR299, AVP, AZU1, MIR26B, MIR25, ATF4, PIK3CD-AS1, MIR34B, MIR34C, MIR302C, ARNT, XRCC6P5, GPR166P, ZFAS1, VN1R17P, ARR3, POTEKP, MIAT, TNFSF12-TNFSF13, MIR17HG, MIR99B, ARRB2, STS, MIR93, LINC00997, LINC00511, FENDRR, CCR3, AGTR1, PNCK, RALYL, UNC5D, MIR216B, GPR151, UBE2QL1, ZFP42, SELENOM, MIR942, RBM45, TSACC, MIR708, ATP6V1G3, B3GALT6, PLK5, CLN3, APLNR, CHEK1, PWAR1, BTLA, SYT6, CDKN2B-AS1, DIRAS1, KIF18B, MGAT5B, AKT2, CHI3L2, CLIC1, LAYN, PIWIL4, FRMPD2, CIRBP, FCER1G, KRT72, UBE2F, SLC43A2, CANT1, H4-16, TP53INP1, MED8, MIR885, COL6A3, COL11A1, COL15A1, MYL12B, SLC31A1, HTRA3, RHEBL1, MUC16, TTYH2, DNER, ARRDC1, MIR505, MTG1, COX6B1, AHNAK2, AZIN2, TRIM9, COL4A3, TMEM52B, CNR2, CYP2R1, LARGE2, GSTO2, TWIST2, MRGPRX4, MRGPRX3, CMTM5, LRRC3B, CTHRC1, COL3A1, MIR155HG, MAL2, NLRP3, FGD5, SPINK13, ALKAL1, KLHL35, SNHG15, ABCD1, LYPD5, MAGED4, CAVIN1, CDH9, CDH13, MAGEA9B, DLX6-AS1, NBAT1, CDH16, CDK5, ASPM, MRGPRX1, NCR3, CCR2, ATG9B, TRIM59, ABCA13, MIR645, LINC01138, TMIGD1, CDC25B, SLC16A12, CDC42, CDH2, NDUFS7, CDH5, RAB37, ACTBL2, GPR149, MIR646, MIR660, CDH8, TREML3P, GADL1, CRPPA, RICTOR, STXBP4, DNAJB8, CADM4, LDHD, DNAJB1P1, ADAMTS18, FUT11, GLIS3, MIR766, OXER1, IL27, CENPE, CETN1, RCC1, ASS1P3, SPAAR, TMEM213, AMOT, MIR671, NUDT17, TXLNA, TET3, CTAG1A, SCUBE3, GPRC6A, HOXA11-AS, KDM1B, MARCHF8, CDKN1C, CDO1, UNC5B, NRK, PRSS55, C4orf46, SLC39A11, CENPX, CEACAM5, SRXN1, FLT3, GAL, COL14A1, MAP3K3, VBP1, VASP, UTY, USP1, UQCRFS1, UQCRC1, NR1H2, UGT1A, MCM5, MGAT5, UCN, KITLG, SUMO1, TYK2, TXNRD1, MGP, TUFM, MCM6, VEGFB, TSG101, WNT2, XRCC3, MAX, XPO1, XPNPEP2, XPNPEP1, XIST, MB, WNT11, WNT1, MCM4, NSD2, LAT2, VTN, TRPV1, VIP, MCC, MCM2, MCM3, TTK, CIITA, NDUFA13, MT1A, MMP14, ALDH6A1, TIE1, TIAM1, KLF10, MSMB, MSN, MST1R, MT1H, TLR4, MT1M, MTAP, COX1, MTHFD1, ND3, MTNR1A, MTRR, NR2F2, MMP13, TSPAN7, MIF, FOXO4, TRPC4, TRAF6, TRAF1, CRISP2, TPT1, MAP3K9, KMT2A, TPD52, TP53BP2, TM7SF2, NR3C2, MMP7, TNFRSF1B, TNFRSF1A, TNFAIP6, MMP11, CLEC3B, TMSB4X, YY1, ZFX, ZNF148, CUL1, CDC14B, LGALS9, APOL1, COPS3, YBX3, SLC43A1, LIFR, OGT, LIG4, USO1, CAVIN2, NR0B2, SNHG3, ULK1, LIPA, LMNB1, SPARCL1, H4C14, MKNK1, HSD17B6, ZBTB17, SLC4A4, TNFRSF6B, ADAM9, LCN1, TNFSF12, TNFSF13, LDHC, ABCC3, LETM1, LGALS3BP, LGALS8, EIF3C, EIF3B, IRS2, DYNLL1, SOCS1, NCOA1, AKR1C3, RTCA, H4C13, H4C5, H4C2, AIMP2, MAD2L1, KMT2D, FGF23, CUL5, CUBN, KAT6A, TUSC3, ARHGEF5, MAGEA4, H4C8, MAGEA9, ST8SIA4, FZD5, MAGEB2, MAOB, NAT2, BSND, PRDM2, DPF3, CAPRIN1, CDR3, LSAMP, H4C3, H4C11, H4C12, H4C6, H4C4, H4C1, FZD8, FZD7, FZD4, FZD1, EOMES, BRAP, AXIN2, AXIN1, H4C9, DYSF, LRP2, MUC5AC, TERF2, TERF1, PON1, SAG, PLD2, S100A12, PLOD1, PLOD2, PMAIP1, S100A5, PRRX1, RXRG, PLD1, RXRA, RRM2, RPS15A, RPS6KB1, POU3F2, ROS1, SNORD15A, BRD2, MAPK12, PLCL1, SFRP5, PITX1, PHF2, SERPINA1, SELENOW, SEMG1, SELP, PIK3R2, PIN1, PIP, CXCL5, SRL, CXCL11, CCL22, PITX2, PLAGL1, CCL17, CCL11, CCL7, PLAUR, RNF2, PPP3CA, RIT1, PTPRC, RAC2, PRKDC, RAB27B, RAB27A, PYCR1, MAPK9, PTPRZ1, PTPRD, PTPN6, RHO, KLK7, KLK10, PRTN3, PTGS1, PTGER4, PSEN1, PTCH1, PSMB6, PRKCZ, PRKCE, RAG2, RAP1B, RHEB, RET, PRF1, PRKAR1A, RCVRN, RBP4, RBP2, RBP1, KDM5A, RB1, RASA1, RARRES1, RARB, RARA, RAP2B, RAP2A, RAP1GAP, PGR, SRSF1, TERC, STAT6, NELL1, SYP, SYCP1, NEK1, NELL2, NEU1, STIM1, NFATC1, STAT5B, NEDD8, STAT5A, NFIA, NFIC, SSTR4, NGFR, SRPK1, NME2, SRC, NEFH, NDUFS1, SGK1, MYH9, TEP1, MMUT, PRDX2, MVD, MXI1, ZNF354A, MYCL, TCF3, MYL2, NDUFB6, CEACAM6, ELOA, NBN, NCF2, TCEA1, TBP, NCL, TAPBP, SPINT1, SPINK1, SPG7, SLC3A2, SERPINA5, CHMP1A, SLC9A1, SLC6A8, PDC, SLC6A1, PDGFRA, PDK3, SLC2A5, NOS1, SLC2A4, SLC1A5, ENPP3, ST3GAL2, SHH, FBXW4, SHC1, SH3GL2, PCDHGC3, SLC22A3, PCBP2, PBX1, NOTCH3, SP1, SOX12, SOX5, NRAS, NT5E, NTRK1, ORC2, OTX1, OVOL1, P4HB, PAEP, PAFAH1B1, SMARCA4, SMARCA2, PRDX1, PAPPA, MPDZ, MATN4, DLK1, AVL9, GPR42, GRK5, GPX1, GPX3, GRB2, GRIA4, KIF1B, KDM4C, SETD1B, WWC1, NR3C1, GRM1, GRM4, PDZD2, TPX2, GRM5, ELL2, SIRT2, MCF2L, XCR1, GIP, GNG4, GLI1, GLI2, LPAR3, GNAI1, GNAO1, SRRM2, CABIN1, DAAM2, TRAM1, TRIM2, HEY1, ABCB10, SF3B3, TMED3, GNG7, SIRT5, DICER1, GPI, PLA2R1, MMRN1, ZHX2, IL24, TBC1D8, KIF3A, PTPRT, HCK, HNRNPUL1, HELLS, TPPP, KLK11, SLC27A4, MLXIP, HFE, COPS5, HGFAC, CKAP4, STIP1, HIC1, PRDX3, HLA-B, HAS1, CORO1A, WDR45, NUDT5, CXCL2, CHSY1, OIP5, ACOT7, GPR182, PARK7, PDIA3, GSK3A, GSN, MSH6, PTENP1, GTF2H4, MAP4K1, BAZ1A, GZMB, PSIP1, H2AX, GPC3, TMEFF2, DHRS4, PSMD10, MYLIP, PYCARD, UBE2T, FLNB, ATAD2, HIPK2, COMMD5, NOB1, TMEM176B, MLANA, DLL1, IGHV1-12, PCLO, SGSM3, FRK, STK39, RPS6KA6, FRZB, FLNA, CARD10, SGK3, EHD2, FGB, FGFR1, F11R, GEMIN4, DEF6, ATP6V0A4, DELEC1, SYCP3, CD209, GRHL1, NOP53, FGFR4, PSAT1, VEGFD, UBIAD1, GPSM2, FKBP4, FOXI1, TOX3, FTH1, RBMS3, SOSTDC1, PRPF31, POLDIP2, CHD5, GGT1, LRIG1, KANK2, GH1, GHR, RCHY1, FUT3, RNF19A, PART1, GHRH, GHSR, PISD, C3CER1, CADM1, RAB38, GDF9, DGCR5, PHGDH, FBXO22, FUT4, KDSR, SIGLEC8, HSPB7, GABPB1, B4GALNT1, GAPDH, DMAC2L, GAS1, B3GAT1, FOXP1, NSG1, USP21, GATA1, GATA2, GREM1, LATS2, GADD45G, HLA-E, LBP, INSRR, IMPA2, NRXN3, SLC9A3R1, IDO1, INSR, TCEAL1, CD163, TRIP10, IRF1, TSIX, MSC, IRF5, ISG20, MTA2, XPR1, ITGA2B, LRRFIP1, ARHGEF2, COX5A, GRAP2, KIF20B, MAGED1, CXCL14, TP53I3, SCAMP1, TBPL1, GDF15, TNFRSF9, ADAMTS1, ADAMTS2, NAPSA, NTN1, RASAL2, FHL5, EIF2AK3, IL17A, GSTO1, FOXK2, NCR1, ILF3, LPAR2, TMSB10, ITGA9, KIF11, KHK, FOXH1, TIMELESS, FUBP1, KLK2, KLRC1, ARHGEF7, PER2, KIFC1, PCSK7, CDK5R1, KAT2B, CCN4, KPNA2, LAIR1, IL18R1, LAMP2, LASP1, SELENBP1, LIMD1, NOL3, F2RL3, NEURL1, ITGAE, ITGB2, ITGB8, ITK, MTA1, RGN, JAG2, PKMYT1, CLDN1, JAK3, PIAS2, SLC7A6, SLC7A7, JUN, KCNH2, KCNJ1, APOBEC3B, WTAP, FGL2, HSF1, NPC2, HOXD3, HP, HRAS, ANP32B, RNASEH2A, AGFG1, HRES1, NXF1, RBCK1, GPNMB, PRMT5, HSP90AA1, NDC80, RACK1, MYL9, DNAJB1, NDST1, AHSA1, MYL12A, NFE2L3, EBP, ADAM28, HMGCR, HMGA1, HMMR, HSPH1, FOXA1, HNRNPA1, USP39, TNFSF13B, HOXC11, GNA13, HNRNPK, HOXA3, HOXA5, IGF2BP1, NPRL2, HOXA11, PDPN, NOD1, TUBB3, HTC2, TNFSF15, GNE, HDAC6, SRA1, IGFBP5, IGFBP6, RCE1, NR1I3, MED12, GAB2, CNPY2, IL1RN, RAPGEF5, KMT2B, IL15, DCAF1, UBE3C, SDC3, RIN1, ABCB6, IGFBP4, KIF20A, ARL4C, IAPP, TNIP1, DLEU1, STAG1, IDH1, SPRY2, STX6, PLIN3, CTDSPL, IDUA, IGF2, TSHZ1, MBNL2, EBI3, IGFBP2, NAMPT, OPTN, NAT1