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Alastrim
Wikipedia
Classification D ICD - 10 : B03 ICD - 9-CM : 050.1 MeSH : D012899 v t e Skin infections , symptoms and signs related to viruses DNA virus Herpesviridae Alpha HSV Herpes simplex Herpetic whitlow Herpes gladiatorum Herpes simplex keratitis Herpetic sycosis Neonatal herpes simplex Herpes genitalis Herpes labialis Eczema herpeticum Herpetiform esophagitis Herpes B virus B virus infection VZV Chickenpox Herpes zoster Herpes zoster oticus Ophthalmic zoster Disseminated herpes zoster Zoster-associated pain Modified varicella-like syndrome Beta Human herpesvirus 6 / Roseolovirus Exanthema subitum Roseola vaccinia Cytomegalic inclusion disease Gamma KSHV Kaposi's sarcoma Poxviridae Ortho Variola Smallpox Alastrim MoxV Monkeypox CPXV Cowpox VV Vaccinia Generalized vaccinia Eczema vaccinatum Progressive vaccinia Buffalopox Para Farmyard pox : Milker's nodule Bovine papular stomatitis Pseudocowpox Orf Sealpox Other Yatapoxvirus : Tanapox Yaba monkey tumor virus MCV Molluscum contagiosum Papillomaviridae HPV Wart / plantar wart Heck's disease Genital wart giant Laryngeal papillomatosis Butcher's wart Bowenoid papulosis Epidermodysplasia verruciformis Verruca plana Pigmented wart Verrucae palmares et plantares BPV Equine sarcoid Parvoviridae Parvovirus B19 Erythema infectiosum Reticulocytopenia Papular purpuric gloves and socks syndrome Polyomaviridae Merkel cell polyomavirus Merkel cell carcinoma RNA virus Paramyxoviridae MeV Measles Togaviridae Rubella virus Rubella Congenital rubella syndrome ("German measles" ) Alphavirus infection Chikungunya fever Picornaviridae CAV Hand, foot, and mouth disease Herpangina FMDV Foot-and-mouth disease Boston exanthem disease Ungrouped Asymmetric periflexural exanthem of childhood Post-vaccination follicular eruption Lipschütz ulcer Eruptive pseudoangiomatosis Viral-associated trichodysplasia Gianotti–Crosti syndrome v t e Eradication of infectious diseases Eradication of human diseases Successful Smallpox / Alastrim ( Eradication of smallpox ) Underway (global) Dracunculiasis ( Eradication of dracunculiasis ) Poliomyelitis ( Eradication of poliomyelitis ) Malaria ( Eradication of malaria ) Yaws ( Eradication of yaws ) Underway (regional) Hookworm Lymphatic filariasis Measles vaccine epidemiology Rubella Trachoma Onchocerciasis Syphilis Rabies Eradication of agricultural diseases Successful Rinderpest ( Eradication of rinderpest ) Underway Ovine rinderpest Bovine spongiform encephalopathy Eradication programs Global Global Polio Eradication Initiative Global Certification Commission Malaria Eradication Scientific Alliance Regional United States Boll Weevil Eradication Program National Malaria Eradication Program India India National PolioPlus Pulse Polio Poliomyelitis in Pakistan Every Last Child The Final Inch Related topics Globalization and disease Mathematical modelling of disease Pandemic Transmission horizontal vertical Vaccination Zoonosis
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Renal Glycosuria
Wikipedia
External links [ edit ] Classification D ICD - 10 : E74.8 ICD - 9-CM : 271.4 OMIM : 233100 MeSH : D006030 DiseasesDB : 29130 External resources eMedicine : ped/1991 Media related to Renal glycosuria at Wikimedia Commons v t e Inborn error of carbohydrate metabolism : monosaccharide metabolism disorders Including glycogen storage diseases (GSD) Sucrose , transport (extracellular) Disaccharide catabolism Congenital alactasia Sucrose intolerance Monosaccharide transport Glucose-galactose malabsorption Inborn errors of renal tubular transport ( Renal glycosuria ) Fructose malabsorption Hexose → glucose Monosaccharide catabolism Fructose : Essential fructosuria Fructose intolerance Galactose / galactosemia : GALK deficiency GALT deficiency / GALE deficiency Glucose ⇄ glycogen Glycogenesis GSD type 0 (glycogen synthase deficiency) GSD type IV (Andersen's disease, branching enzyme deficiency) Adult polyglucosan body disease (APBD) Glycogenolysis Extralysosomal: GSD type III (Cori's disease, debranching enzyme deficiency) GSD type VI (Hers' disease, liver glycogen phosphorylase deficiency) GSD type V (McArdle's disease, myophosphorylase deficiency) GSD type IX (phosphorylase kinase deficiency) Lysosomal ( LSD ): GSD type II (Pompe's disease, glucosidase deficiency) Glucose ⇄ CAC Glycolysis MODY 2 / HHF3 GSD type VII (Tarui's disease, phosphofructokinase deficiency) Triosephosphate isomerase deficiency Pyruvate kinase deficiency Gluconeogenesis PCD Fructose bisphosphatase deficiency GSD type I (von Gierke's disease, glucose 6-phosphatase deficiency) Pentose phosphate pathway Glucose-6-phosphate dehydrogenase deficiency Transaldolase deficiency 6-phosphogluconate dehydrogenase deficiency Other Hyperoxaluria Primary hyperoxaluria Pentosuria Aldolase A deficiency v t e Genetic disorder , membrane: Solute carrier disorders 1-10 SLC1A3 Episodic ataxia 6 SLC2A1 De Vivo disease SLC2A5 Fructose malabsorption SLC2A10 Arterial tortuosity syndrome SLC3A1 Cystinuria SLC4A1 Hereditary spherocytosis 4 / Hereditary elliptocytosis 4 SLC4A11 Congenital endothelial dystrophy type 2 Fuchs' dystrophy 4 SLC5A1 Glucose-galactose malabsorption SLC5A2 Renal glycosuria SLC5A5 Thyroid dyshormonogenesis type 1 SLC6A19 Hartnup disease SLC7A7 Lysinuric protein intolerance SLC7A9 Cystinuria 11-20 SLC11A1 Crohn's disease SLC12A3 Gitelman syndrome SLC16A1 HHF7 SLC16A2 Allan–Herndon–Dudley syndrome SLC17A5 Salla disease SLC17A8 DFNA25 21-40 SLC26A2 Multiple epiphyseal dysplasia 4 Achondrogenesis type 1B Recessive multiple epiphyseal dysplasia Atelosteogenesis, type II Diastrophic dysplasia SLC26A4 Pendred syndrome SLC35C1 CDOG 2C SLC39A4 Acrodermatitis enteropathica SLC40A1 African iron overload see also solute carrier family
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Impetigo Herpetiformis
Wikipedia
External links [ edit ] Classification D ICD - 10 : L40.1 ( ILDS L40.120) ICD - 9-CM : 694.3 DiseasesDB : 33949 v t e Papulosquamous disorders Psoriasis Pustular Generalized pustular psoriasis ( Impetigo herpetiformis ) Acropustulosis / Pustulosis palmaris et plantaris ( Pustular bacterid ) Annular pustular psoriasis Localized pustular psoriasis Other Guttate psoriasis Psoriatic arthritis Psoriatic erythroderma Drug-induced psoriasis Inverse psoriasis Napkin psoriasis Seborrheic-like psoriasis Parapsoriasis Pityriasis lichenoides ( Pityriasis lichenoides et varioliformis acuta , Pityriasis lichenoides chronica ) Lymphomatoid papulosis Small plaque parapsoriasis ( Digitate dermatosis , Xanthoerythrodermia perstans ) Large plaque parapsoriasis ( Retiform parapsoriasis ) Other pityriasis Pityriasis rosea Pityriasis rubra pilaris Pityriasis rotunda Pityriasis amiantacea Other lichenoid Lichen planus configuration Annular Linear morphology Hypertrophic Atrophic Bullous Ulcerative Actinic Pigmented site Mucosal Nails Peno-ginival Vulvovaginal overlap synromes with lichen sclerosus with lupus erythematosis other: Hepatitis-associated lichen planus Lichen planus pemphigoides Other Lichen nitidus Lichen striatus Lichen ruber moniliformis Gianotti–Crosti syndrome Erythema dyschromicum perstans Idiopathic eruptive macular pigmentation Keratosis lichenoides chronica Kraurosis vulvae Lichen sclerosus Lichenoid dermatitis Lichenoid reaction of graft-versus-host disease v t e Pathology of pregnancy , childbirth and the puerperium Pregnancy Pregnancy with abortive outcome Abortion Ectopic pregnancy Abdominal Cervical Interstitial Ovarian Heterotopic Embryo loss Fetal resorption Molar pregnancy Miscarriage Stillbirth Oedema , proteinuria and hypertensive disorders Gestational hypertension Pre-eclampsia HELLP syndrome Eclampsia Other, predominantly related to pregnancy Digestive system Acute fatty liver of pregnancy Gestational diabetes Hepatitis E Hyperemesis gravidarum Intrahepatic cholestasis of pregnancy Integumentary system / dermatoses of pregnancy Gestational pemphigoid Impetigo herpetiformis Intrahepatic cholestasis of pregnancy Linea nigra Prurigo gestationis Pruritic folliculitis of pregnancy Pruritic urticarial papules and plaques of pregnancy (PUPPP) Striae gravidarum Nervous system Chorea gravidarum Blood Gestational thrombocytopenia Pregnancy-induced hypercoagulability Maternal care related to the fetus and amniotic cavity amniotic fluid Oligohydramnios Polyhydramnios Braxton Hicks contractions chorion / amnion Amniotic band syndrome Chorioamnionitis Chorionic hematoma Monoamniotic twins Premature rupture of membranes Obstetrical bleeding Antepartum placenta Circumvallate placenta Monochorionic twins Placenta accreta Placenta praevia Placental abruption Twin-to-twin transfusion syndrome Labor Amniotic fluid embolism Cephalopelvic disproportion Dystocia Shoulder dystocia Fetal distress Locked twins Nuchal cord Obstetrical bleeding Postpartum Pain management during childbirth placenta Placenta accreta Preterm birth Postmature birth Umbilical cord prolapse Uterine inversion Uterine rupture Vasa praevia Puerperal Breastfeeding difficulties Low milk supply Cracked nipples Breast engorgement Childbirth-related posttraumatic stress disorder Diastasis symphysis pubis Postpartum bleeding Peripartum cardiomyopathy Postpartum depression Postpartum psychosis Postpartum thyroiditis Puerperal fever Puerperal mastitis Other Concomitant conditions Diabetes mellitus Systemic lupus erythematosus Thyroid disorders Maternal death Sexual activity during pregnancy Category
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Hirschsprung Disease
Medlineplus
Hirschsprung disease can occur in combination with other conditions, such as Waardenburg syndrome, type IV; Mowat-Wilson syndrome; or congenital central hypoventilation syndrome. These cases are described as syndromic. Hirschsprung disease can also occur without other conditions, and these cases are referred to as isolated or nonsyndromic.
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Pes Anserine Bursitis
Wikipedia
External links [ edit ] Classification D External resources eMedicine : article/308694 v t e Soft tissue disorders Capsular joint Synoviopathy Synovitis / Tenosynovitis Calcific tendinitis Stenosing tenosynovitis Trigger finger De Quervain syndrome Transient synovitis Ganglion cyst osteochondromatosis Synovial osteochondromatosis Plica syndrome villonodular synovitis Giant-cell tumor of the tendon sheath Bursopathy Bursitis Olecranon Prepatellar Trochanteric Subacromial Achilles Retrocalcaneal Ischial Iliopsoas Synovial cyst Baker's cyst Calcific bursitis Noncapsular joint Symptoms Ligamentous laxity Hypermobility Enthesopathy / Enthesitis / Tendinopathy upper limb Adhesive capsulitis of shoulder Impingement syndrome Rotator cuff tear Golfer's elbow Tennis elbow lower limb Iliotibial band syndrome Patellar tendinitis Achilles tendinitis Calcaneal spur Metatarsalgia Bone spur other/general: Tendinitis / Tendinosis Nonjoint Fasciopathy Fasciitis : Plantar Nodular Necrotizing Eosinophilic Fibromatosis / contracture Dupuytren's contracture Plantar fibromatosis Aggressive fibromatosis Knuckle pads v t e Inflammation Symptoms Flushing (Rubor) Fever (Calor) Swelling (Tumor) Pain (Dolor) Malaise Mechanism Acute Plasma-derived mediators Bradykinin complement C3 C5a MAC coagulation Factor XII Plasmin Thrombin Cell-derived mediators preformed: Lysosome granules biogenic amines Histamine Serotonin synthesized on demand: cytokines IFN-γ IL-8 TNF-α IL-1 eicosanoids Leukotriene B4 Prostaglandins Nitric oxide Kinins Chronic Macrophage Epithelioid cell Giant cell Granuloma Other Acute-phase reaction Vasodilation Increased vascular permeability Exudate Leukocyte extravasation Chemotaxis Tests Full blood count Leukocytosis C-reactive protein Erythrocyte sedimentation rate General Lymphadenopathy List of inflammed body part states
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Hypophysitis
Wikipedia
. ^ http://pathology2.jhu.edu/hypophysitis/theprognfollowup.cfm ^ http://pathology2.jhu.edu/hypophysitis/histricalnotes.cfm v t e Pituitary disease Hyperpituitarism Anterior Acromegaly Hyperprolactinaemia Pituitary ACTH hypersecretion Posterior SIADH General Nelson's syndrome Hypophysitis Hypopituitarism Anterior Kallmann syndrome Growth hormone deficiency Hypoprolactinemia ACTH deficiency / Secondary adrenal insufficiency GnRH insensitivity FSH insensitivity LH/hCG insensitivity Posterior Neurogenic diabetes insipidus General Empty sella syndrome Pituitary apoplexy Sheehan's syndrome Lymphocytic hypophysitis Pituitary adenoma
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Brodie Abscess
Wikipedia
External links [ edit ] Classification D ICD - 10 : M86.8 ICD - 9-CM : 730.1 External resources eMedicine : article/1248682 v t e Bone and joint disease Bone Inflammation endocrine : Osteitis fibrosa cystica Brown tumor infection : Osteomyelitis Sequestrum Involucrum Sesamoiditis Brodie abscess Periostitis Vertebral osteomyelitis Metabolic Bone density Osteoporosis Juvenile Osteopenia Osteomalacia Paget's disease of bone Hypophosphatasia Bone resorption Osteolysis Hajdu–Cheney syndrome Ainhum Gorham's disease Other Ischaemia Avascular necrosis Osteonecrosis of the jaw Complex regional pain syndrome Hypertrophic pulmonary osteoarthropathy Nonossifying fibroma Pseudarthrosis Stress fracture Fibrous dysplasia Monostotic Polyostotic Skeletal fluorosis bone cyst Aneurysmal bone cyst Hyperostosis Infantile cortical hyperostosis Osteosclerosis Melorheostosis Pycnodysostosis Joint Chondritis Relapsing polychondritis Other Tietze's syndrome Combined Osteochondritis Osteochondritis dissecans Child leg: hip Legg–Calvé–Perthes syndrome tibia Osgood–Schlatter disease Blount's disease foot Köhler disease Sever's disease spine Scheuermann's_disease arm: wrist Kienböck's disease elbow Panner disease
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Trilogy Of Fallot
Wikipedia
External links [ edit ] Classification D ICD - 10 : Q21.3 ICD9 = 746.09 , 746.8 ( CDC/BPA 746.84) MeSH : D014286 v t e Congenital heart defects Heart septal defect Aortopulmonary septal defect Double outlet right ventricle Taussig–Bing syndrome Transposition of the great vessels dextro levo Persistent truncus arteriosus Aortopulmonary window Atrial septal defect Sinus venosus atrial septal defect Lutembacher's syndrome Ventricular septal defect Tetralogy of Fallot Atrioventricular septal defect Ostium primum Consequences Cardiac shunt Cyanotic heart disease Eisenmenger syndrome Valvular heart disease Right pulmonary valves stenosis insufficiency absence tricuspid valves stenosis atresia Ebstein's anomaly Left aortic valves stenosis insufficiency bicuspid mitral valves stenosis regurgitation Other Underdeveloped heart chambers right left Uhl anomaly Dextrocardia Levocardia Cor triatriatum Crisscross heart Brugada syndrome Coronary artery anomaly Anomalous aortic origin of a coronary artery Ventricular inversion This article about a congenital malformation is a stub .
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Canine Cognitive Dysfunction
Wikipedia
When these precautions are taken, the dog will have a higher chance of living longer with as little effects of CCD as possible. [7] See also [ edit ] Feline cognitive dysfunction References [ edit ] ^ "Cognitive Dysfunction Syndrome in Dogs" . Pets.webmd.com . Retrieved 2014-01-28 . ^ a b Andrea Menashe (2013-10-30). "Pet Talk: Canine Cognitive Dysfunction Syndrome much more manageable when caught early" . ... Retrieved 2014-01-28 . ^ "Cognitive Dysfunction Syndrome in Dogs" (PDF) . Lap of Love Educational Pet Disease Series. ... "Therapeutic agents for the treatment of cognitive dysfunction syndrome in senior dogs". Progress in Neuro-Psychopharmacology and Biological Psychiatry . 29 (3): 471–479. doi : 10.1016/j.pnpbp.2004.12.012 .
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Rhinolith
Wikipedia
External links [ edit ] Classification D ICD - 10 : J34.8 ICD - 9-CM : 478.19 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 disease , disorder, or medical condition is a stub .
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Combined Oxidative Phosphorylation Deficiency 32
Omim
Brain imaging shows T2-weighted abnormalities in the basal ganglia and brainstem consistent with Leigh syndrome (256000). Patient cells showed decreased activities of mitochondrial respiratory chain complexes, I, III, and IV, as well as impaired mitochondrial translation (summary by Lake et al., 2017). ... The sixth child (patient S4) presented at 10 days of age with poor feeding and neurologic symptoms, such as no eye contact, hypotonia, dystonia, and pyramidal syndrome of the lower limbs; he died at age 8.5 months. ... Brain imaging in all patients showed abnormal T2-weighted signals in the brainstem and basal ganglia, consistent with Leigh syndrome. Muscle biopsies showed variably decreased activities of mitochondrial respiratory complexes I, III, and IV. ... INHERITANCE - Autosomal recessive HEAD & NECK Head - Microcephaly (in some patients) Face - Coarse facial features (in some patients) Eyes - Dysconjugate eye movements - Strabismus - Exotropia - Ptosis - Nystagmus - Optic atrophy (in 1 patient) RESPIRATORY - Abnormal breathing pattern (in some patients) ABDOMEN Gastrointestinal - Poor feeding - Gastroesophageal reflux - Constipation SKELETAL - Joint contractures Spine - Kyphoscoliosis MUSCLE, SOFT TISSUES - Hypotonia - Decreased activities of mitochondrial respiratory complexes I, III, and IV NEUROLOGIC Central Nervous System - Delayed psychomotor development - Developmental regression - Lack of speech - Inability to walk - Spasticity - Dystonia - Choreoathetoid movements - Abnormal T2-weighted signals in the basal ganglia and brainstem - Leigh syndrome Peripheral Nervous System - Hyperreflexia METABOLIC FEATURES - Lactic acidosis LABORATORY ABNORMALITIES - Increased serum lactate - Increased CSF lactate - Combined oxidative phosphorylation deficiency MISCELLANEOUS - Onset in first days or months of life - Progressive disorder - May result in early death MOLECULAR BASIS - Caused by mutation in the mitochondrial ribosomal protein S34 gene (MRPS34, 611994.0001 ). ▲ Close
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Hidrocystoma
Wikipedia
Contents 1 Additional images 2 See also 3 References 4 External links Additional images [ edit ] Eccrine hydrocystoma See also [ edit ] Syringoma Acrospiroma Seborrheic keratosis List of cutaneous conditions List of cutaneous neoplasms associated with systemic syndromes References [ edit ] ^ a b c Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... External links [ edit ] Classification D ICD - 10 : D23.1 ICD-O : 8404/0 MeSH : D018251 DiseasesDB : 33660 SNOMED CT : 80549000 External resources eMedicine : derm/35 v t e Glandular and epithelial cancer Epithelium Papilloma / carcinoma Small-cell carcinoma Combined small-cell carcinoma Verrucous carcinoma Squamous cell carcinoma Basal-cell carcinoma Transitional cell carcinoma Inverted papilloma Complex epithelial Warthin's tumor Thymoma Bartholin gland carcinoma Glands Adenomas / adenocarcinomas Gastrointestinal tract: Linitis plastica Familial adenomatous polyposis pancreas Insulinoma Glucagonoma Gastrinoma VIPoma Somatostatinoma Cholangiocarcinoma Klatskin tumor Hepatocellular adenoma / Hepatocellular carcinoma Urogenital Renal cell carcinoma Endometrioid tumor Renal oncocytoma Endocrine Prolactinoma Multiple endocrine neoplasia Adrenocortical adenoma / Adrenocortical carcinoma Hürthle cell Other/multiple Neuroendocrine tumor Carcinoid Adenoid cystic carcinoma Oncocytoma Clear-cell adenocarcinoma Apudoma Cylindroma Papillary hidradenoma Adnexal and skin appendage sweat gland Hidrocystoma Syringoma Syringocystadenoma papilliferum Cystic, mucinous, and serous Cystic general Cystadenoma / Cystadenocarcinoma Mucinous Signet ring cell carcinoma Krukenberg tumor Mucinous cystadenoma / Mucinous cystadenocarcinoma Pseudomyxoma peritonei Mucoepidermoid carcinoma Serous Ovarian serous cystadenoma / Pancreatic serous cystadenoma / Serous cystadenocarcinoma / Papillary serous cystadenocarcinoma Ductal, lobular, and medullary Ductal carcinoma Mammary ductal carcinoma Pancreatic ductal carcinoma Comedocarcinoma Paget's disease of the breast / Extramammary Paget's disease Lobular carcinoma Lobular carcinoma in situ Invasive lobular carcinoma Medullary carcinoma Medullary carcinoma of the breast Medullary thyroid cancer Acinar cell Acinic cell carcinoma v t e Cancers of skin and associated structures Glands Sweat gland Eccrine Papillary eccrine adenoma Eccrine carcinoma Eccrine nevus Syringofibroadenoma Spiradenoma Apocrine Cylindroma Dermal cylindroma Syringocystadenoma papilliferum Papillary hidradenoma Hidrocystoma Apocrine gland carcinoma Apocrine nevus Eccrine / apocrine Syringoma Hidradenoma or Acrospiroma / Hidradenocarcinoma Ceruminous adenoma Sebaceous gland Nevus sebaceous Muir–Torre syndrome Sebaceous carcinoma Sebaceous adenoma Sebaceoma Sebaceous nevus syndrome Sebaceous hyperplasia Mantleoma Hair Pilomatricoma / Malignant pilomatricoma Trichoepithelioma Multiple familial trichoepithelioma Solitary trichoepithelioma Desmoplastic trichoepithelioma Generalized trichoepithelioma Trichodiscoma Trichoblastoma Fibrofolliculoma Trichilemmoma Trichilemmal carcinoma Proliferating trichilemmal cyst Giant solitary trichoepithelioma Trichoadenoma Trichofolliculoma Dilated pore Isthmicoma Fibrofolliculoma Perifollicular fibroma Birt–Hogg–Dubé syndrome Hamartoma Basaloid follicular hamartoma Folliculosebaceous cystic hamartoma Folliculosebaceous-apocrine hamartoma Nails Neoplasms of the nailbed This Epidermal nevi, neoplasms, cysts article is a stub .
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Calcaneal Spur
Wikipedia
External links [ edit ] Calcaneal spur at Curlie Classification D ICD - 10 : M77.3 ICD - 9-CM : 726.73 MeSH : D036982 DiseasesDB : 10467 SNOMED CT : 55260003 Wikimedia Commons has media related to Calcaneal spur . v t e Soft tissue disorders Capsular joint Synoviopathy Synovitis / Tenosynovitis Calcific tendinitis Stenosing tenosynovitis Trigger finger De Quervain syndrome Transient synovitis Ganglion cyst osteochondromatosis Synovial osteochondromatosis Plica syndrome villonodular synovitis Giant-cell tumor of the tendon sheath Bursopathy Bursitis Olecranon Prepatellar Trochanteric Subacromial Achilles Retrocalcaneal Ischial Iliopsoas Synovial cyst Baker's cyst Calcific bursitis Noncapsular joint Symptoms Ligamentous laxity Hypermobility Enthesopathy / Enthesitis / Tendinopathy upper limb Adhesive capsulitis of shoulder Impingement syndrome Rotator cuff tear Golfer's elbow Tennis elbow lower limb Iliotibial band syndrome Patellar tendinitis Achilles tendinitis Calcaneal spur Metatarsalgia Bone spur other/general: Tendinitis / Tendinosis Nonjoint Fasciopathy Fasciitis : Plantar Nodular Necrotizing Eosinophilic Fibromatosis / contracture Dupuytren's contracture Plantar fibromatosis Aggressive fibromatosis Knuckle pads
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Giant Condyloma Acuminatum
Wikipedia
PMID: 28396786 v t e Skin infections , symptoms and signs related to viruses DNA virus Herpesviridae Alpha HSV Herpes simplex Herpetic whitlow Herpes gladiatorum Herpes simplex keratitis Herpetic sycosis Neonatal herpes simplex Herpes genitalis Herpes labialis Eczema herpeticum Herpetiform esophagitis Herpes B virus B virus infection VZV Chickenpox Herpes zoster Herpes zoster oticus Ophthalmic zoster Disseminated herpes zoster Zoster-associated pain Modified varicella-like syndrome Beta Human herpesvirus 6 / Roseolovirus Exanthema subitum Roseola vaccinia Cytomegalic inclusion disease Gamma KSHV Kaposi's sarcoma Poxviridae Ortho Variola Smallpox Alastrim MoxV Monkeypox CPXV Cowpox VV Vaccinia Generalized vaccinia Eczema vaccinatum Progressive vaccinia Buffalopox Para Farmyard pox : Milker's nodule Bovine papular stomatitis Pseudocowpox Orf Sealpox Other Yatapoxvirus : Tanapox Yaba monkey tumor virus MCV Molluscum contagiosum Papillomaviridae HPV Wart / plantar wart Heck's disease Genital wart giant Laryngeal papillomatosis Butcher's wart Bowenoid papulosis Epidermodysplasia verruciformis Verruca plana Pigmented wart Verrucae palmares et plantares BPV Equine sarcoid Parvoviridae Parvovirus B19 Erythema infectiosum Reticulocytopenia Papular purpuric gloves and socks syndrome Polyomaviridae Merkel cell polyomavirus Merkel cell carcinoma RNA virus Paramyxoviridae MeV Measles Togaviridae Rubella virus Rubella Congenital rubella syndrome ("German measles" ) Alphavirus infection Chikungunya fever Picornaviridae CAV Hand, foot, and mouth disease Herpangina FMDV Foot-and-mouth disease Boston exanthem disease Ungrouped Asymmetric periflexural exanthem of childhood Post-vaccination follicular eruption Lipschütz ulcer Eruptive pseudoangiomatosis Viral-associated trichodysplasia Gianotti–Crosti syndrome This infection-related cutaneous condition article is a stub .
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Attention-Deficit/hyperactivity Disorder
Medlineplus
Affected individuals may also have autism spectrum disorder, which is characterized by impaired communication and social interaction, or Tourette syndrome, which is a disorder characterized by repetitive and involuntary movements or noises called tics. ... In these instances, ADHD is usually one of several features of a syndrome that affects multiple parts of the body. ... When ADHD is a feature of another genetic syndrome, it can be passed on according to the inheritance pattern of that syndrome.DRD5, COMT, DRD4, STS, GRM5, FGD1, AS3MT, MED13, ADGRL3, DRD2, CIC, SLC6A3, TPH2, CHRNA4, GRM7, GIT1, CNR1, TACR1, GRM8, CALY, PTPRD, CHRNB2, GRM1, ZNF292, DHDDS, CHRNA7, GRIN2A, ASTN2, MECP2, UPF3B, PTCHD1, SYP, CACNA1C, FOXP2, ST3GAL3, GJB2, PTEN, ITIH3, FAS, AUTS2, THRB, NTRK2, CPLX2, SLC6A8, DMD, IFNG, PIK3CA, PRKG1, FMR1, SLITRK1, PTPRG, GABRB3, PAH, IQSEC2, SMC3, TRNS2, TRNW, NBN, SEC24C, GTF2IRD1, ARHGEF6, SYNGAP1, NCL, SYNJ1, BAZ1B, BRSK2, PPM1D, HERC2, SEMA3E, IKBKG, CACNA1H, JRK, FEZ1, NOP56, FRMPD4, MID2, ND6, TRNF, MKRN3-AS1, GNB5, RAI1, GPC6, TRNH, GNE, TRNL1, TRNQ, USP9X, TRNS1, MED12, KIF14, ATP2C2, CPLX1, NUAK1, DEAF1, MAGED2, TLK2, HDAC4, SMC1A, PAK3, CHAF1B, AP3B2, SLC6A9, SLC6A4, OCRL, SLC6A2, SLC2A1, SLC1A2, SIM1, SDHA, SCN8A, SCN3A, OPHN1, RXRG, RREB1, RPS20, RPS6KA3, RFC2, RAD21, PTPRF, PRNP, MAPK1, PRKCG, PPP3CA, POLG, PMS2, PMS1, SMPD1, SNAP25, SNRPN, TSC2, ADAM12, TRIM26, PCGF2, MKRN3, ZNF41, ZNF711, YWHAG, CLIP2, PCNT, UBE3A, HIRA, TSC1, SOX5, TRIO, NDN, TSPAN7, IL1RAPL1, TGFBR2, NDP, TCF20, TCF4, TBX1, STXBP1, SPG7, UFD1, VPS13A, ITGA11, AK8, FBXL16, PWAR1, PIWIL4, MUCL3, IRAK1BP1, OSR1, MTFMT, RAB39B, NUS1, CSMD2, C12orf57, ALKBH8, MLIP, SLC9A7, ASCC2, FERMT3, TMEM47, CSRNP3, SEMA6D, PANK2, UBA5, ALG13, SPAG16, ARV1, CSMD1, SEMA4A, CXorf56, VPS13B, SPRED1, BCORL1, ARX, LINC01572, OBI1-AS1, P2RX5-TAX1BP3, BORCS7-ASMT, KDM4A-AS1, TAF9BP2, SNORD116-1, PWRN1, LINC00461, MIR137HG, USP27X, SFTA2, MIR99AHG, CEP85L, KIF7, HCN1, TUBB2B, ZNF81, SNORD115-1, ZNF615, LAMA1, SLC13A5, ASPM, JMJD1C, CEP112, CFAP221, ARID2, PIEZO2, SORCS2, PUF60, SH3KBP1, MLH3, CYFIP2, TBL2, SETBP1, TENM4, NECAP1, PARS2, SH2B1, SIN3A, NIPBL, FTSJ1, NPAP1, CDK20, ZFPM2, ADNP, MED13L, SYNE1, SZT2, SATB2, ND4, SORCS3, NT5C2, SHANK2, FAN1, TRAK1, NLGN1, CNKSR2, SRPX2, ZNRD1, TBC1D24, TAX1BP3, SLC4A10, C12orf4, HDAC8, MCTP2, CHD7, DHTKD1, PI4K2B, ACOXL, MAP11, SETD5, PHIP, NSUN2, DYM, CNNM2, RBFOX1, MAGEL2, WWOX, MPP6, ACTL6B, WAC, RSRC1, CRBN, ZDHHC9, MLXIPL, WDPCP, NTM, SCAPER, ND5, AARS1, ND1, IPW, BDNF, BMPR1A, BRCA2, CACNA1A, CACNA1B, IGF1, CACNB2, DNM1, HTR2A, HTR1B, HSPG2, HOXA2, HLA-DPB2, HLA-DMB, HIVEP1, BCR, ITGAE, AGTR2, ATP6V1A, LIMK1, LIG4, LHCGR, ANK3, KRAS, KIF11, KIF5B, ARF1, ARSD, KCNB1, KCNA2, ARVCF, ITPR3, STT3A, RERE, CHD2, CLCN4, HDC, HCFC1, CSNK2A1, FLII, FLI1, FGF12, ACSL4, EMP2, ELN, EEF1A2, DBH, DPP6, DDX3X, TIMM8A, DHCR7, DYNC1I2, DLG3, GABRA1, GABRB2, GABRG2, GRIA4, GTF2I, MSH6, CLTC, GRIN2D, COL2A1, COL11A2, GP1BB, GATA4, GNAS, GNAQ, GLUD1, CREBBP, CRKL, GDI1, ABCD1, DYNC1H1, MOBP, MEF2C, ADCY2, KMT2A, MAOB, ADRA2A, MAOA, MSH2, MANBA, EPCAM, COX1, MAN2A2, MLH1, COX2, COX3, MITF, DRD1, CDH13, CLOCK, ELK3, CYP2D6, DNTT, MTHFR, NTF3, STX1A, WASF2, ADRA1A, EPHB1, SLC9A9, NGF, CHPT1, HTR1A, LOC110806262, RSS, NR3C1, SSTR4, LPAR2, ADRA2B, HTR2C, SMS, ADRA2C, MC4R, GTS, BAIAP2, GRIN2B, CXCR6, REM1, DDC, DRD3, LOC107987479, EDNRA, NOS1, GPR42, NPY, BRS3, TPH1, NET1, ACKR3, HCRT, VEGFA, DISC1, SHANK3, CES1, ABCB10P1, WASF1, DIRAS2, NR4A2, IMPACT, STUB1, ADIPOQ, CHRNA3, ZNF804A, AMPH, SLC1A3, VAMP2, ANKK1, SHBG, MIRLET7D, ADORA2A, CDK5, FLRT3, DCDC2, NDRG2, CFP, HLA-DRB1, PART1, PER2, ATXN1, CRP, TSPAN31, NCAM1, DTNBP1, LOC102723407, GUCY2C, CNTNAP2, SCLY, RBM12, ADHD5, OPN1SW, BAG3, LOC102724971, OXTR, CHRNA5, ERICD, SPN, COA7, F2R, APOE, CYBC1, NANS, DCLK1, GAD1, SOD1, DNAAF4, TERF1, PRS, GNPAT, GRIA1, INSRR, BTBD9, C4B, SLC9A6, INS, IL1B, IL1RN, SLC2A3, NPSR1, IL5, IL6, TRH, TPO, TERC, KRT7, IL10, DNMT3B, BDNF-AS, SYN3, EBPL, RFC1, CAT, SYT1, BCHE, INTS8, MTR, TAL1, PIK3CG, POMC, POLR3A, ZFPM2-AS1, CSF2, PSC, APP, ACACA, CSE1L, FBXO33, CRY1, SLC30A10, CREM, NPNT, MIR5692B, PIDD1, TTC12, CYP3A4, PRTG, NCAN, AGA, IPO11, NAT8L, COL6A4P1, ALDH2, FEZF1, ALB, AKT1, GAL, NR0B1, ASCC1, DLG2, SPOCK3, STIN2-VNTR, DLX4, LOC390714, AMH, BRINP1, CCHCR1, CTNND1, TRIT1, ELFN1, CYP2B6, P4HTM, CYP2D7, CNTN5, PLA1A, AMPD1, GPRC5B, CPT2, THRA1/BTR, DAPK3, LOC105379528, ADRB2, CNTFR, ADM, BPIFA2, CBS, PPP1R1B, KYAT1, CCT, LMAN2L, KCNIP4, CD38, CD40, AGT, NRSN1, CD79A, CDH11, MIR34B, MIR320A, RNF122, MICALL2, NTPCR, STXBP5-AS1, AVP, ZGPAT, MIR148B, RBM45, SYT2, BHMT, DCD, THEM4, ADHD2, ADHD4, XKR4, MIR34C, MIR378A, NDUFAF2, SLC39A13, CASP3, CLEC19A, ZBBX, ATM, EAF2, KLK3, DGKH, TMX2-CTNND1, MIR107, CNTN1, OXER1, ARNTL, PRXL2C, APRT, FEZF1-AS1, LXN, C9orf72, DNAJC12, DYX8, KYAT3, ASH1L, CORD1, KIDINS220, NUFIP2, LUCAT1, MIR138-1, MBOAT7, FTO, ADRA1B, ASMT, NSD1, CHRNB3, SLC39A8, CHRNB4, CLTA, MIR3171, MIR142, LINC01672, HAMP, DPP10, LRRC7, SNORC, NUDT3, NT5C, VDR, SLC18A2, SLC16A1, KCNC1, KCNJ5, KCNJ6, KCNJ11, SLC6A1, SLC5A4, SKI, LAIR1, SDHD, LAMB2, CCL11, SCT, LAMC2, LGALS3, SCD, ATXN7, S100B, FADS1, LMNA, REG1A, RARA, SMN1, SMN2, SNCA, THAS, IL1A, TXN, TWIST1, PHLDA2, IL2, TNR, TSPAN8, THRSP, THRA, THBS3, TH, ITPA, IL16, ABCA4, ITGA1, SULT2A1, STXBP3, CDKL5, STATH, STAT6, SST, SRY, LMX1B, RAB3A, PEX2, NGFR, PDE4A, PDE2A, MFAP1, PC, PRKN, MFGE8, MIP, OPRM1, NTRK3, NTRK1, NFKB1, PFN1, NF1, NR3C2, MNT, MOG, MYT1, MYO5B, MPP2, MSMB, MTHFD1, MTNR1A, PDE4D, SERPINA1, PTPRN2, PROC, LRP6, LRP5, CYP4F3, PTPRC, PTH, PTGDS, PSPH, PSG5, PSD, RELN, PSPN, PIK3CB, MXD1, PRKCD, PRKCB, PPIA, PON1, MAP1B, MARK1, PMCH, SERPINF2, PIK3CD, IGFALS, VIPR2, KCNIP1, IGF2, RRS1, CYFIP1, FN1, VWA8, GAST, TRIM32, GALR1, GCH1, GFI1, PARK7, HRH3, SEC23IP, NISCH, CORO1A, TRIM31, RAB40B, PDE10A, GPER1, WASF3, NRG3, GRIA2, SH2B2, GRIK5, FKBP5, FHIT, FGF2, EGF, PADI1, ZCCHC4, IGHV3-69-1, IGHV3OR16-7, HTRA2, ZNF544, CNTN6, DOCK3, AGO1, EDA, EIF4EBP1, SYNM, TPSG1, PRPF6, EPHA5, FRRS1L, CADM1, SMUG1, OTP, KCNH3, ERBB2, FAAH, CIB1, CACNG2, RIDA, HPRT1, HK1, KALRN, SELENBP1, CHRNA6, ARHGEF7, HP, NRP1, NRP2, LIN7A, B4GALT2, USO1, PKMYT1, BHLHE40, HRC, HTR1D, HTR1E, ZMYM2, TRIM25, HTR3A, HTR4, HTR5A, HTR6, ARTN, PDLIM1, GPHN, HFE, PSMD14, TSHZ1, RASGRP1, BCL2L10, SLC12A6, GSK3B, BMS1, GYPA, GUCY2D, CARTPT, BCAR1, LGI1, ADAMTS2, HGF, ITM2B, FADS2, NRXN1, TGM5, PDLIM7, GPR50, DLGAP1, MTA2, H3P40
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Monostotic Fibrous Dysplasia
Wikipedia
External links [ edit ] Classification D ICD - 10 : M85.0 ICD - 9-CM : 733.29 MeSH : D005358 DiseasesDB : 32262 External resources Orphanet : 93277 v t e Bone and joint disease Bone Inflammation endocrine : Osteitis fibrosa cystica Brown tumor infection : Osteomyelitis Sequestrum Involucrum Sesamoiditis Brodie abscess Periostitis Vertebral osteomyelitis Metabolic Bone density Osteoporosis Juvenile Osteopenia Osteomalacia Paget's disease of bone Hypophosphatasia Bone resorption Osteolysis Hajdu–Cheney syndrome Ainhum Gorham's disease Other Ischaemia Avascular necrosis Osteonecrosis of the jaw Complex regional pain syndrome Hypertrophic pulmonary osteoarthropathy Nonossifying fibroma Pseudarthrosis Stress fracture Fibrous dysplasia Monostotic Polyostotic Skeletal fluorosis bone cyst Aneurysmal bone cyst Hyperostosis Infantile cortical hyperostosis Osteosclerosis Melorheostosis Pycnodysostosis Joint Chondritis Relapsing polychondritis Other Tietze's syndrome Combined Osteochondritis Osteochondritis dissecans Child leg: hip Legg–Calvé–Perthes syndrome tibia Osgood–Schlatter disease Blount's disease foot Köhler disease Sever's disease spine Scheuermann's_disease arm: wrist Kienböck's disease elbow Panner disease This article about a disease of musculoskeletal and connective tissue is a stub .
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Anasarca
Wikipedia
Contents 1 Signs and symptoms 1.1 physical appearance 1.2 physical manifestations 2 Cause 3 Diagnosis 3.1 Testing 4 References 5 External links Signs and symptoms [ edit ] physical appearance [ edit ] Can include: · periorbital edema " eye puffiness " · perioral edema · upper extremity edema · ascites · lower extremity edema · pre-tibial edema · pedal edema physical manifestations [ edit ] Can include: · impaired vision, difficulty opening eyes · shortness of breath (SOB), dyspnea on exertion (DOE), orthopnea · chest pain · extreme discomfort · debilitation Cause [ edit ] Causes include liver failure , [2] kidney failure , [3] right-sided heart failure , nephrotic syndrome , [4] protein-losing enteropathies , [5] severe protein deficiency , [6] and capillary leak syndrome . [7] Anasarca is often caused by a decreased oncotic pressure . ... Retrieved 2020-07-02 . ^ "Nephrotic syndrome - Symptoms and causes" . Mayo Clinic . ... "Case Report: Uncontrolled Anasarca: CapillaryLeak Syndrome" . The Medicine Forum . The Medicine Forum: Vol. 17 , Article 8. 17 . doi : 10.29046/TMF.017.1.009 .
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Deafness, Autosomal Recessive 2
Omim
Allelic disorders include autosomal dominant deafness-11 (DFNA11; 601317) and Usher syndrome type IB (USH1B; see 276900). Clinical Features Guilford et al. (1994) reported a consanguineous family from southern Tunisia in which 22 individuals had autosomal recessive nonsyndromic sensorineural deafness. ... Zina et al. (2001) concluded that some patients in this Tunisian family had features consistent with Usher syndrome type IB. The findings suggested that other factors must modulate the expression of the phenotype. ... The sh1 phenotype differs from that of Usher syndrome in humans by the absence of retinal degeneration. ... INHERITANCE - Autosomal recessive HEAD & NECK Ears - Hearing loss, sensorineural, prelingual - Hearing loss affects all frequencies NEUROLOGIC Central Nervous System - Vestibular dysfunction - Vertigo MISCELLANEOUS - Onset usually at birth, but may occur later - Allelic disorder to autosomal dominant nonsyndromic sensorineural deafness (DFNA11, 601317 ) and Usher syndrome type IB ( 276900 ) MOLECULAR BASIS - Caused by mutation in the myosin VIIA gene (MYO7A, 276903.0007 ) ▲ Close
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Myxoma, Intracardiac
Omim
The first family included a brother and a sister, both with acromegaly, suggesting a syndromal form of myxoma. Farah (1994) stated that 'none of the family members had skin tumors, abnormal pigmentation, other tumors or evidence of endocrine disease.' ... Thus, it seems likely that the sibs in fact had Carney syndrome. Indeed, the sister would appear to have been case 14 of Carney et al. (1985). ... However, unlike sporadic cardiac myxomas, which most often occur as isolated single lesions in middle-aged women and which are usually amenable to surgical resection, syndromic cardiac myxomas exhibit no age or sex preference and may present as multiple concurrent lesions in any cardiac chamber. ... A son and a daughter of hers had atrial myxoma and a 12-year-old son had died suddenly after having cardiac symptoms consistent with myxoma. No signs indicative of Carney syndrome were found. Dandolu et al. (1995) suggested autosomal dominant inheritance.