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Terson Syndrome
Wikipedia
Terson syndrome Eye anatomy(vitreous humor indicated) Specialty Ophthalmology Terson syndrome or Terson's syndrome is the occurrence of a vitreous hemorrhage of the human eye in association with subarachnoid hemorrhage . ... Its likely cause is a rapid increase in ICP. [1] The classic presentation is in the subhyaloidal space, which is beneath the posterior vitreous face and in front of the retina. [ citation needed ] In subarachnoid hemorrhage, 13% of patients have Terson's syndrome, which is associated with more severe SAH (higher Hunt-Hess score, a marker of severity), and risk of death is significantly increased. [2] The first known report of the association was by the German ophthalmologist Moritz Litten in 1881. [3] Still, French ophthalmologist Albert Terson's name is more commonly associated with the condition after a report by his hand from 1900. [4] References [ edit ] ^ Medele RJ, Stummer W, Mueller AJ, Steiger HJ, Reulen HJ (1998). "Terson's syndrome in subarachnoid hemorrhage and severe brain injury accompanied by acutely raised intracranial pressure". ... "A systematic review of Terson's syndrome: frequency and prognosis after subarachnoid haemorrhage" .
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Polyradiculoneuropathy
Wikipedia
Polyradiculoneuropathy Specialty Neurology Polyradiculoneuropathy describes a condition in which polyneuropathy and polyradiculopathy occur together. An example is Guillain–Barré syndrome . Treatment with a single course of intravenous immunoglobulin (IVIG) infusions has been demonstrated to be a potentially effective treatment (reported to have caused prolonged remission in a case associated with systemic lupus ( Systemic lupus erythematosus ) ). [1] References [ edit ] ^ P Lesprit; F Mouloud; F Bierling; A Schaeffer; P Cesaro; C Brun-Buisson; B Godeau (1996). ... External links [ edit ] Classification D ICD - 9-CM : 357.0 MeSH : D011129 Polyradiculoneuropathy at the US National Library of Medicine Medical Subject Headings (MeSH) 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 This article about a medical condition affecting the nervous system is a stub .
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Musculoskeletal Abnormality
Wikipedia
They can be due to deformity or malformation . [1] An example is Klippel–Feil syndrome . Although present at birth, some only become obvious postnatally. [2] References [ edit ] ^ "Introduction: Congenital Craniofacial and Musculoskeletal Abnormalities: Merck Manual Professional" . ^ "UNSW Embryology- Musculoskeletal System - Abnormalities" . ... External links [ edit ] Classification D ICD - 10 : Q65 - Q79 ICD - 9-CM : 754 - 756 MeSH : D009139 v t e Congenital malformations and deformations of musculoskeletal system / musculoskeletal abnormality Appendicular limb / dysmelia Arms clavicle / shoulder Cleidocranial dysostosis Sprengel's deformity Wallis–Zieff–Goldblatt syndrome hand deformity Madelung's deformity Clinodactyly Oligodactyly Polydactyly Leg hip Hip dislocation / Hip dysplasia Upington disease Coxa valga Coxa vara knee Genu valgum Genu varum Genu recurvatum Discoid meniscus Congenital patellar dislocation Congenital knee dislocation foot deformity varus Club foot Pigeon toe valgus Flat feet Pes cavus Rocker bottom foot Hammer toe Either / both fingers and toes Polydactyly / Syndactyly Webbed toes Arachnodactyly Cenani–Lenz syndactylism Ectrodactyly Brachydactyly Stub thumb reduction deficits / limb Acheiropodia Ectromelia Phocomelia Amelia Hemimelia multiple joints Arthrogryposis Larsen syndrome RAPADILINO syndrome Axial Skull and face Craniosynostosis Scaphocephaly Oxycephaly Trigonocephaly Craniofacial dysostosis Crouzon syndrome Hypertelorism Hallermann–Streiff syndrome Treacher Collins syndrome other Macrocephaly Platybasia Craniodiaphyseal dysplasia Dolichocephaly Greig cephalopolysyndactyly syndrome Plagiocephaly Saddle nose Vertebral column Spinal curvature Scoliosis Klippel–Feil syndrome Spondylolisthesis Spina bifida occulta Sacralization Thoracic skeleton ribs : Cervical Bifid sternum : Pectus excavatum Pectus carinatum This genetic disorder article is a stub .
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Gastroptosis
Wikipedia
External links [ edit ] Classification D ICD - 10 : K31.8 ICD - 9-CM : 537.5 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 NDL : 00564016 This human digestive system article is a stub .
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Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome
Wikipedia
Autosomal recessive genetic condition Camptodactyly-arthropathy-coxa vara-pericarditis syndrome Other names Pericarditis-arthropathy-camptodactyly syndrome Camptodactyly-arthropathy-coxa vara-pericarditis syndrome is a rare autosomal recessive genetic condition due to a mutation in the gene proteoglycan 4 ( PRG4 ) – a mucin -type glycoprotein that acts as a lubricant for the cartilage surfaces. ... Contents 1 Presentation 2 Genetics 3 Diagnosis 3.1 Laboratory 3.2 Radiology 4 Management 5 References 6 External links Presentation [ edit ] This condition was first described in 1986. [1] and is a syndrome of camptodactyly , arthropathy , coxa vara and pericarditis . [2] It may also include congenital cataracts . [3] The cause of this syndrome was discovered in 1999. [4] Children with this syndrome often present with a joint effusion that is cool and resistant to anti-inflammatory therapy. ... You can help by adding to it . ( January 2018 ) References [ edit ] ^ Bulutlar G, Yazici H, Ozdogan H, Schreuder I (1986) A familial syndrome of pericarditis, arthritis, camptodactyly and coxa vara. Arthritis Rheum 29:436–438 ^ a b Offiah AC, Woo P, Prieur AM, Hasson N, Hall CM (2005) Camptodactyly-arthropathy-coxa vara-pericarditis syndrome versus juvenile idiopathic arthropathy. AJR Am J Roentgenol 185(2):522-529 ^ Akawi NA, Ali BR, Al-Gazali L (2012) A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.
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Duodenitis
Wikipedia
External links [ edit ] Classification D ICD - 10 : K29.8 ICD - 9-CM : 535.6 MeSH : D004382 SNOMED CT : 72007001 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
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Obturator Hernia
Wikipedia
External links [ edit ] Classification D ICD - 10 : K45 ICD - 9-CM : 553.8 MeSH : D006553 DiseasesDB : 29334 SNOMED CT : 60627008 External resources eMedicine : article/775630 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 This article about a disease , disorder, or medical condition is a stub .
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Spondyloperipheral Dysplasia
Wikipedia
Find sources: "Spondyloperipheral dysplasia" – news · newspapers · books · scholar · JSTOR ( August 2010 ) ( Learn how and when to remove this template message ) Spondyloperipheral dysplasia Other names Spondyloperipheral dysplasia-short ulna syndrome Spondyloperipheral dysplasia has an autosomal dominant pattern of inheritance . ... PMID 8723097 . ^ Online Mendelian Inheritance in Man (OMIM): 120140 This article incorporates public domain text from Spondyloperipheral dysplasia at NLM Genetics Home Reference External links [ edit ] Spondyloperipheral dysplasia short ulna at NIH 's Office of Rare Diseases Classification D OMIM : 271700 MeSH : C535799 DiseasesDB : 34165 SNOMED CT : 702339001 External resources Orphanet : 1856 v t e Diseases of collagen , laminin and other scleroproteins Collagen disease COL1 : Osteogenesis imperfecta Ehlers–Danlos syndrome, types 1, 2, 7 COL2 : Hypochondrogenesis Achondrogenesis type 2 Stickler syndrome Marshall syndrome Spondyloepiphyseal dysplasia congenita Spondyloepimetaphyseal dysplasia, Strudwick type Kniest dysplasia (see also C2/11 ) COL3 : Ehlers–Danlos syndrome, types 3 & 4 Sack–Barabas syndrome COL4 : Alport syndrome COL5 : Ehlers–Danlos syndrome, types 1 & 2 COL6 : Bethlem myopathy Ullrich congenital muscular dystrophy COL7 : Epidermolysis bullosa dystrophica Recessive dystrophic epidermolysis bullosa Bart syndrome Transient bullous dermolysis of the newborn COL8: Fuchs' dystrophy 1 COL9: Multiple epiphyseal dysplasia 2, 3, 6 COL10: Schmid metaphyseal chondrodysplasia COL11: Weissenbacher–Zweymüller syndrome Otospondylomegaepiphyseal dysplasia (see also C2/11 ) COL17: Bullous pemphigoid COL18: Knobloch syndrome Laminin Junctional epidermolysis bullosa Laryngoonychocutaneous syndrome Other Congenital stromal corneal dystrophy Raine syndrome Urbach–Wiethe disease TECTA DFNA8/12, DFNB21 see also fibrous proteins
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Immune Disorder
Wikipedia
Common symptoms include low-grade fever and feeling tired . [4] Often symptoms come and go. [4] List of some autoimmune disorders [ edit ] Main article: Autoimmune disease Lupus Scleroderma Certain types of hemolytic anemia Vasculitis Type 1 diabetes Graves' disease Rheumatoid arthritis Multiple sclerosis (although it is thought to be an immune-mediated process) Goodpasture syndrome Pernicious anemia Some types of myopathy Lyme disease (Late) Immunodeficiencies [ edit ] Main article: immunodeficiency Primary immune deficiency diseases are those caused by inherited genetic mutations. ... Immunodeficient patients may less frequently develop abscesses of their internal organs, autoimmune or rheumatologic and gastrointestinal problems. [6] Primary immune deficiencies Severe combined immunodeficiency (SCID) DiGeorge syndrome Hyperimmunoglobulin E syndrome (also known as Job's Syndrome) Common variable immunodeficiency (CVID): B-cell levels are normal in circulation but with decreased production of IgG throughout the years, so it is the only primary immune disorder that presents onset in the late teens years. ... Classical recurrent infection from catalase positive bacteria and fungi. Wiskott–Aldrich syndrome (WAS) Autoimmune lymphoproliferative syndrome (ALPS) Hyper IgM syndrome : X-linked disorder that causes a deficiency in the production of CD40 ligand on activated T-cells. ... Retrieved 31 August 2011 . ^ http://www.merckmanuals.com/home/immune_disorders.html External links [ edit ] Classification D ICD - 10 : D80 - D89 ICD - 9-CM : 273 , 279 MeSH : D007154 Immune disorder at Curlie Eczema and Immune Disorders at This Podcast Has Autism v t e Lymphoid and complement disorders causing immunodeficiency Primary Antibody / humoral ( B ) Hypogammaglobulinemia X-linked agammaglobulinemia Transient hypogammaglobulinemia of infancy Dysgammaglobulinemia IgA deficiency IgG deficiency IgM deficiency Hyper IgM syndrome ( 1 2 3 4 5 ) Wiskott–Aldrich syndrome Hyper-IgE syndrome Other Common variable immunodeficiency ICF syndrome T cell deficiency ( T ) thymic hypoplasia : hypoparathyroid ( Di George's syndrome ) euparathyroid ( Nezelof syndrome Ataxia–telangiectasia ) peripheral: Purine nucleoside phosphorylase deficiency Hyper IgM syndrome ( 1 ) Severe combined (B+T) x-linked: X-SCID autosomal: Adenosine deaminase deficiency Omenn syndrome ZAP70 deficiency Bare lymphocyte syndrome Acquired HIV/AIDS Leukopenia : Lymphocytopenia Idiopathic CD4+ lymphocytopenia Complement deficiency C1-inhibitor ( Angioedema / Hereditary angioedema ) Complement 2 deficiency / Complement 4 deficiency MBL deficiency Properdin deficiency Complement 3 deficiency Terminal complement pathway deficiency Paroxysmal nocturnal hemoglobinuria Complement receptor deficiency v t e Immunoproliferative immunoglobulin disorders PCDs / PP Plasmacytoma Multiple myeloma ( Plasma cell leukemia ) MGUS IgM ( Macroglobulinemia / Waldenström's macroglobulinemia ) heavy chain ( Heavy chain disease ) light chain ( Primary amyloidosis ) Other hypergammaglobulinemia Cryoglobulinemia 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 Biology portal Medicine portal
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Cerebellar Hypoplasia
Wikipedia
External links [ edit ] Classification D ICD - 10 : Q04.3 ICD - 9-CM : 742.2 OMIM : 213000 MeSH : C562568 External resources Orphanet : 1398 Cerebellar-Hypoplasia at NINDS Cerebellar hypoplasia at NIH 's Office of Rare Diseases v t e Symptoms , signs and syndromes associated with lesions of the brain and brainstem Brainstem Medulla (CN 8, 9, 10, 12) Lateral medullary syndrome/Wallenberg PICA Medial medullary syndrome/Dejerine ASA Pons (CN 5, 6, 7, 8) Upper dorsal pontine syndrome/Raymond-Céstan syndrome Lateral pontine syndrome ( AICA ) (lateral) Medial pontine syndrome / Millard–Gubler syndrome / Foville's syndrome ( basilar ) Locked-in syndrome Internuclear ophthalmoplegia One and a half syndrome Midbrain (CN 3, 4) Weber's syndrome ventral peduncle, PCA Benedikt syndrome ventral tegmentum, PCA Parinaud's syndrome dorsal, tumor Claude's syndrome Other Alternating hemiplegia Cerebellum Latearl Dysmetria Dysdiadochokinesia Intention tremor ) Medial Cerebellar ataxia Basal ganglia Chorea Dystonia Parkinson's disease Cortex ACA syndrome MCA syndrome PCA syndrome Frontal lobe Expressive aphasia Abulia Parietal lobe Receptive aphasia Hemispatial neglect Gerstmann syndrome Astereognosis Occipital lobe Bálint's syndrome Cortical blindness Pure alexia Temporal lobe Cortical deafness Prosopagnosia Thalamus Thalamic syndrome Other Upper motor neuron lesion AphasiaVLDLR, MAB21L1, ATAD3A, PIGU, NMNAT2, OPHN1, CASK, RELN, ITPR1, RARS2, POMT2, PAFAH1B1, VRK1, PI4KA, TSEN54, WNT1, ADGRG1, FKRP, POMT1, PMM2, DKC1, WDR37, GMPPB, MSTO1, SLC25A24, PSAT1, INPP5K, SEPSECS, WDR60, MBTPS2, PIGT, RTEL1, MKS1, PIGG, NDE1, KCTD3, DISC1, GPSM2, CCDC22, AFG3L2, B4GAT1, CIT, POLR3A, MAN1B1, USP18, TREX1, RAB3GAP1, MAST1, MAPK8IP3, PMPCA, RHOBTB2, KIAA0556, CAMTA1, BICD2, MACF1, ATP6V0A2, C2CD3, PHGDH, TINF2, PCLO, CEP55, ABAT, CWF19L1, TOE1, POMK, TMEM107, MFSD2A, POMGNT2, ATCAY, TUBGCP6, WDR34, MARS2, TBCK, TP53RK, WDR81, ATRIP, B3GALNT2, CEP120, VPS13B, TAPT1, TUBB, PTF1A, FLG-AS1, ARSI, TUBB2B, CRPPA, KIAA1109, TRAPPC9, POMGNT1, EPG5, FLVCR2, PACS1, AHCY, FRMD4A, VAC14, POLR3B, ERMARD, SNX14, WDR35, IFT80, SLC25A19, TSEN2, PIEZO2, ROBO3, SIL1, ACD, CARS2, ROGDI, DYNC2H1, CSPP1, TCTN2, COASY, GJB6, STAG2, YME1L1, RAC1, FGFR2, FLG, FLNA, GJB2, GLI3, GPX4, BRF1, L1CAM, LAMB1, MUSK, MYO5A, NDUFA6, NFIX, NONO, PARN, CHMP1A, TUBB3, PIGA, PLG, FGFR1, FKTN, ERF, CDK5, ASNS, ATP2B3, ATP5F1A, ATP6V1A, ATP6V1E1, BUB1B, CACNA1A, CDC42, CENPE, ERCC6, CENPF, COL3A1, COL4A1, CSF1R, CTNNA2, DAG1, DHFR, ERCC1, MAP2K2, OCLN, TERT, LARGE1, KIAA0586, TWIST1, SLC35A2, CEP104, ATG5, RNF113A, CACNA1G, FIG4, USP9X, RBM10, ARID1A, EOMES, PLA2G6, DPM2, TERC, GPAA1, SON, SMARCB1, RXYLT1, RBBP8, STUB1, GPHN, SIX3, SLC25A1, SLC1A3, SMARCE1, KIF14, HDAC6, CHD7, TUBA1A, WDR73, EXOSC3, AIRE, TPPP, HESX1, LHX4, ASPM, RMDN2, CAT, ZNF423, TRIP13, PTK2, LHX3, DCX, EN2, RMDN3, PRL, POU1F1, SYBU, EXOSC9, NTRK1, THOC2, SOD1, RMDN1, SRD5A1, PDX1, IGHD, WNT5A, ZIC1, GHRHR, GAP43, PROP1, ATAD3B, ZIC4, PDGFRB
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Strømme Syndrome
Wikipedia
Rare genetic condition involving intestinal atresia, eye abnormalities and microcephaly Strømme syndrome Other names Stromme syndrome, apple-peel intestinal atresia–ocular anomalies–microcephaly syndrome, [1] jejunal atresia–microcephaly–ocular anomalies syndrome, [1] apple peel syndrome with microcephaly and ocular anomalies, [2] jejunal atresia with microcephaly and ocular anomalies, [2] (formerly) primary ciliary dyskinesia 31 (CILD31) [2] Female infant with Strømme syndrome showing microcephaly Pronunciation Norwegian pronunciation: [ˈstrœ̂mːə] Specialty Medical genetics Symptoms Apple-peel intestinal atresia , underdeveloped eyes, microcephaly with developmental delay; sometimes additional symptoms or fewer symptoms [2] [3] Causes Genetic (autosomal recessive mutation in CENPF ) [2] [3] Diagnostic method Based on symptoms, genetic testing [4] Prognosis Not yet certain. ... They proposed that it constituted a new syndrome. [2] [8] Later studies by Slee and Goldblatt (1996), [5] Shanske et al. (2002), [13] Bellini et al. (2002) [11] and others observed other patients with similar symptoms who appeared to have the syndrome. [2] In 2008, Van Bever et al. proposed that the syndrome be named after Strømme, after encountering another patient who seemed to have the syndrome. [2] [9] In 2015, Waters et al. conducted a genetic analysis on a British family in which four foetuses had miscarried with symptoms of a ciliopathy . ... Retrieved 27 September 2018 . ^ a b c d e f g h i Filges, Isabel; Stromme, Petter (2020). "CUGC for Stromme syndrome and CENPF-related disorders" . ... (October 1996). "Further evidence for a syndrome of "apple peel" intestinal atresia, ocular anomalies and microcephaly". ... PMID 28401041 . ^ a b Shanske, Alan L.; Gurland, Judith E.; Mbekeani, Joyce N.; Bello, Jacqueline A.; Campbell, Deborah; Kleinhaus, Sylvain (January 2002). "Possible new syndrome of microcephaly with cortical migration defects, Peters anomaly and multiple intestinal atresias: a multiple vascular disruption syndrome".
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Iliotibial Band Syndrome
Wikipedia
"Iliotibial band friction syndrome—A systematic review". Manual Therapy . 12 (3): 200–8. doi : 10.1016/j.math.2006.08.004 . ... Retrieved 2019-11-17 . ^ a b c d Neal, Bradley (2016). "Iliotibial Band Syndrome: A Narrative Review". Co-Kinetic Journal . 67 : 16–20 – via EBSCO host. ^ "Iliotibial Band Syndrome: Background, Epidemiology, Functional Anatomy" . 2019-11-10. ... PMID 12649036 . ^ Flynn, Sharon H.; Khaund, Razib (2005-04-15). "Iliotibial Band Syndrome: A Common Source of Knee Pain" . ... (August 1992). "Iliotibial Band Syndrome". Sports Medicine . 14 (2): 144–148. doi : 10.2165/00007256-199214020-00005 . ... G. (23 December 2012). "Iliotibial Band Syndrome in Runners". Sports Medicine . 42 (11): 969–992. doi : 10.1007/BF03262306 .
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Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome
Omim
Rodes et al. (1987) reported a family in which 2 brothers and a sister were affected with HHH syndrome. One patient had progressive spastic paraparesis. ... Dionisi Vici et al. (1987) found reports of 23 patients with HHH syndrome in the literature, only 1 of whom showed symptoms as a neonate. ... Salvi et al. (2001) reported a follow-up on 8 Italian patients who had been diagnosed with HHH syndrome. Age at onset ranged from infancy to 18 years. ... They referred to a case of untreated HHH syndrome in the mother being associated with a mentally retarded offspring. Shih et al. (1992) described neonatal death in the HHH syndrome and successful prenatal diagnosis of the disorder in a subsequent pregnancy in this family.
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Wells Syndrome
Gard
Wells syndrome is a rare eosinophilic disorder that primarily affects the skin. ... The exact underlying cause of Wells syndrome is currently unknown; however, some scientists believe that it may be an autoimmune reaction . Oral or topical corticosteroids are commonly used to treat Wells syndrome, although antifungal drugs, antibiotics, immunosuppressants , and/or antihistamines have also been used with varying degrees of success.
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Genoa Syndrome
Gard
Genoa syndrome is a rare condition that primarily affects the brain and skull. ... They later develop craniosynostosis (the premature closure of one or more of the fibrous joints between the bones of the skull before brain growth is complete). Genoa syndrome also appears to be associated with other skeletal abnormalities, including those of the hands, and distinctive facial features. ... Some reports suggest that Genoa syndrome may be inherited in an autosomal recessive manner.
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Crane-Heise Syndrome
Orphanet
Crane-Heise syndrome is a very rare syndrome characterized by poorly mineralized calvarium, facial dysmorphism, vertebral abnormalities and absent clavicles. ... Prognosis Prognosis is poor; the syndrome is almost always lethal soon after birth.
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Semicircular Canal Dehiscence Syndrome
Orphanet
Semicircular canal dehiscence (SCD) syndrome is a rare otorhinolaryngologic disease characterized by the uni- or bilateral dehiscence of the bone(s) overlying the superior (most common), lateral or posterior semicircular canal(s). Patients present audiological (autophony, aural fullness, conductive hearing loss, pulsatile tinnitus) and/or vestibular symptoms (sound or pressure-evoked oscillopsia or vertigo, characteristic vertical-torsional eye movements), depending on which semicircular canal is affected. Posterior SCD syndrome is associated with high-riding jugular bulb and fibrous dysplasia, while lateral SCD syndrome is associated with chronic otitis media and cholesteatoma, with or without audiological and vestibular symptoms.
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Hypertrichosis-Acromegaloid Facial Appearance Syndrome
Orphanet
Hypertrichosis-acromegaloid facial appearance syndrome (HAFF) is a very rare multiple congenital abnormality syndrome manifesting from birth with progressive hypertrichosis congenita terminalis (thick scalp hair extending onto the forehead with generalized increased body hair) associated with a typical acromegaloid facial appearance (thick eyebrows, prominent supraorbital ridges, broad nasal bridge, anteverted nares, long and large philtrum, and prominent mouth with full lips) appearing during childhood. HAFF seems to belong to a spectrum of phenotypes with the clinically overlapping acromegaloid facial appearance syndrome and hypertrichotic osteochondrodysplasia, Cantù type (see these terms).
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Ankyloblepharon
Wikipedia
The currently accepted theory is that this condition is due to temporary epithelial arrest and rapid mesenchymal proliferation, allowing union of eyelids at abnormal positions. [5] Systemic associations [ edit ] Congenital ankyloblepharon is seen in association with: Hay-Wells syndrome : Ankyloblepharon-Ectodermal dysplasia-Clefting (AEC) syndrome also known as Hay-Wells syndrome is a rare autosomal dominant disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft palate and/or cleft lip. [6] Curly Hair-Ankyloblepharon-Nail Disease (CHAND) syndrome: it is a clinical variant of AEC syndrome. It is also known as Baughman syndrome. [6] Trisomy 18 (Edwards syndrome): AFA may be seen in association with Trisomy 18 . [7] Popliteal pterygium syndrome (PPS): Popliteal pterygium syndrome (PPS) is a rare autosomal dominant disorder, first described by Trelat in 1869. ... CS1 maint: multiple names: authors list ( link ) ^ a b Sabin Sahu. "Hay-Wells syndrome: Report of a rare disorder with dental management" . ... "Ankyloblepharon filiforme adnatum in trisomy 18 (Edwards's syndrome)" . British Journal of Ophthalmology . 69 (6): 471–473. doi : 10.1136/bjo.69.6.471 . ... PMID 4005216 . ^ Muhammad Qasim and Mahmood Shaukat (2012). "Popliteal Pterygium Syndrome: A Rare Entity" . Apsp Journal of Case Reports . 3 (1): 5.
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Dyssomnia
Wikipedia
The major three groups, along with the group types, include: [1] : 15 Intrinsic sleep disorders [1] : 15 idiopathic hypersomnia , narcolepsy , periodic limb movement disorder , restless legs syndrome , obstructive sleep apnea , central sleep apnea syndrome , sleep state misperception , psychophysiologic insomnia, recurrent hypersomnia, post-traumatic hypersomnia, central alveolar hypoventilation syndrome, Extrinsic sleep disorders – 13 disorders recognized, including [1] : 16 alcohol-dependent sleep disorder, food allergy insomnia , inadequate sleep routine. Circadian rhythm sleep disorders , both intrinsic and extrinsic – 6 disorders recognized, including [1] : 16 advanced sleep phase syndrome , delayed sleep phase syndrome , jetlag , shift work sleep disorder . ... External links [ edit ] Classification D ICD - 9-CM : 307.47 , 780.56 MeSH : D020920 v t e Mental and behavioral disorders Adult personality and behavior Gender dysphoria Ego-dystonic sexual orientation Paraphilia Fetishism Voyeurism Sexual maturation disorder Sexual relationship disorder Other Factitious disorder Munchausen syndrome Intermittent explosive disorder Dermatillomania Kleptomania Pyromania Trichotillomania Personality disorder Childhood and learning Emotional and behavioral ADHD Conduct disorder ODD Emotional and behavioral disorders Separation anxiety disorder Movement disorders Stereotypic Social functioning DAD RAD Selective mutism Speech Stuttering Cluttering Tic disorder Tourette syndrome Intellectual disability X-linked intellectual disability Lujan–Fryns syndrome Psychological development ( developmental disabilities ) Pervasive Specific Mood (affective) Bipolar Bipolar I Bipolar II Bipolar NOS Cyclothymia Depression Atypical depression Dysthymia Major depressive disorder Melancholic depression Seasonal affective disorder Mania Neurological and symptomatic Autism spectrum Autism Asperger syndrome High-functioning autism PDD-NOS Savant syndrome Dementia AIDS dementia complex Alzheimer's disease Creutzfeldt–Jakob disease Frontotemporal dementia Huntington's disease Mild cognitive impairment Parkinson's disease Pick's disease Sundowning Vascular dementia Wandering Other Delirium Organic brain syndrome Post-concussion syndrome Neurotic , stress -related and somatoform Adjustment Adjustment disorder with depressed mood Anxiety Phobia Agoraphobia Social anxiety Social phobia Anthropophobia Specific social phobia Specific phobia Claustrophobia Other Generalized anxiety disorder OCD Panic attack Panic disorder Stress Acute stress reaction PTSD Dissociative Depersonalization disorder Dissociative identity disorder Fugue state Psychogenic amnesia Somatic symptom Body dysmorphic disorder Conversion disorder Ganser syndrome Globus pharyngis Psychogenic non-epileptic seizures False pregnancy Hypochondriasis Mass psychogenic illness Nosophobia Psychogenic pain Somatization disorder Physiological and physical behavior Eating Anorexia nervosa Bulimia nervosa Rumination syndrome Other specified feeding or eating disorder Nonorganic sleep Hypersomnia Insomnia Parasomnia Night terror Nightmare REM sleep behavior disorder Postnatal Postpartum depression Postpartum psychosis Sexual dysfunction Arousal Erectile dysfunction Female sexual arousal disorder Desire Hypersexuality Hypoactive sexual desire disorder Orgasm Anorgasmia Delayed ejaculation Premature ejaculation Sexual anhedonia Pain Nonorganic dyspareunia Nonorganic vaginismus Psychoactive substances, substance abuse and substance-related Drug overdose Intoxication Physical dependence Rebound effect Stimulant psychosis Substance dependence Withdrawal Schizophrenia , schizotypal and delusional Delusional Delusional disorder Folie à deux Psychosis and schizophrenia-like Brief reactive psychosis Schizoaffective disorder Schizophreniform disorder Schizophrenia Childhood schizophrenia Disorganized (hebephrenic) schizophrenia Paranoid schizophrenia Pseudoneurotic schizophrenia Simple-type schizophrenia Other Catatonia Symptoms and uncategorized Impulse control disorder Klüver–Bucy syndrome Psychomotor agitation Stereotypy 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 sclerosis v t e Sleep and sleep disorders Stages of sleep cycles Rapid eye movement (REM) Non-rapid eye movement Slow-wave Brain waves Alpha wave Beta wave Delta wave Gamma wave K-complex Mu rhythm PGO waves Sensorimotor rhythm Sleep spindle Theta wave Sleep disorders Dyssomnia Excessive daytime sleepiness Hypersomnia Insomnia Kleine–Levin syndrome Narcolepsy Night eating syndrome Nocturia Sleep apnea Catathrenia Central hypoventilation syndrome Obesity hypoventilation syndrome Obstructive sleep apnea Periodic breathing Sleep state misperception Circadian rhythm disorders Advanced sleep phase disorder Cyclic alternating pattern Delayed sleep phase disorder Irregular sleep–wake rhythm Jet lag Non-24-hour sleep–wake disorder Shift work sleep disorder Parasomnia Bruxism Nightmare disorder Night terror Periodic limb movement disorder Rapid eye movement sleep behavior disorder Sleepwalking Somniloquy Benign phenomena Dreams Exploding head syndrome Hypnic jerk Hypnagogia / Sleep onset Hypnopompic state Sleep paralysis Sleep inertia Somnolence Nocturnal clitoral tumescence Nocturnal penile tumescence Nocturnal emission Treatment Sleep diary Sleep hygiene Sleep induction Hypnosis Lullaby Somnology Polysomnography Other Sleep medicine Behavioral sleep medicine Sleep study Daily life Bed Bunk bed Daybed Four-poster bed Futon Hammock Mattress Sleeping bag Bed bug Bedding Bedroom Bedtime Bedtime story Bedtime toy Biphasic and polyphasic sleep Chronotype Dream diary Microsleep Mouth breathing Nap Nightwear Power nap Second wind Siesta Sleep and creativity Sleep and learning Sleep deprivation / Sleep debt Sleeping while on duty Sleepover SnoringRAI1, ATXN3, CDKL5, ASXL3, PRNP, MBD5, PIGQ, USP8, VPS35, EPM2A, SLC6A5, TUSC3, AIFM1, SMC3, LHX3, SMC1A, PRSS12, CASK, WFS1, CRADD, HESX1, ATAD3A, SETD5, CISD2, HDAC8, LINS1, TFAP2B, SNCA, SOX2, SOX3, SPR, GATAD2B, STXBP1, TBP, TCF20, THRA, EZR, THRB, NKX2-1, TRHR, TRIO, TSHB, TSHR, C12orf4, FMN2, AIMP1, MED23, SLC18A2, TECR, IQSEC2, SPART, VPS13A, SATB2, DNAJC13, WASHC4, ADNP, FRRS1L, FBXO7, ATXN10, NIPBL, RTTN, SIN3A, GIGYF2, HIBCH, BSCL2, CRBN, DCPS, SLC45A1, TNIK, PNKP, MAN1B1, SLC9A6, NSUN2, GABBR2, SNCAIP, HDAC4, ARNT2, GPHN, CC2D1A, WARS2, DEAF1, WDR45, CORIN, RSRC1, STAG2, KDM5B, WDR4, SEPTIN9, PIGP, LIAS, SMARCC2, SLC2A1, SEPSECS, TRAPPC9, FLT1, METTL23, GBA, GCH1, LRRK2, SLITRK1, GLRA1, GLRB, GLUD2, GNAO1, GNS, GRIK2, LHX4, HDC, HNMT, ST3GAL3, IDUA, FLII, PROKR2, FGFR1, CTNNB1, ADH1C, AGA, ASPA, NHLRC1, MFSD8, STOX1, ARX, DBH, HGSNAT, SIK1, DCTN1, DDC, SARDH, EIF4G1, EML1, B3GALNT2, ATAD1, NDST1, FBXO31, ZC3H14, EHMT1, POU1F1, PPT1, KCNA1, PROP1, SLC25A22, MBOAT7, RAD21, CLIP1, SARS1, CDH23, ATXN2, ATXN8OS, EPG5, SCN2A, CHD8, SGSH, PIGC, NSDHL, PGAP1, OTX2, NR4A2, EDC3, MED25, NEUROD2, NDP, MAPT, LMAN2L, MECP2, TRIM8, NAGLU, KMT2A, CRP, HCRT, COMT, COPD, TIMELESS, APOE, MAOA, IL6, MPPE1, ASPSCR1, NALCN, PLXNA3, PDSS2, CCL4L1, PLF, OPN4, ACHE, REM1, PRSS21, NFKB2, NBN, MEIS1, LAMC2, IL1B, IFNA2, HCRTR2, GLI2, GH1, GDF1, FMR1, FLG, FANCC, ESR1, ACE, CSN1S1, CSF2, CSF1R, CSE1L, CECR, CCT, BBS2, AGRP, NHS, PAX6, PER1, VEGFA, CERS1, IGSF6, CCL4L2, KL, ARTN, PER3, SRPX, ACP5, XPO1, VIP, UMOD, PNN, TNF, STAC, CCL4, SCD, ATXN1, BRD2, REN, PSG3, PSG2, PRL, PAX8