A list of diseases in the English wikipedia. A disease is an abnormal condition of the body or mind that causes discomfort, dysfunction, or distress to the person afflicted or those in contact with the person. ...

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z A listing of diseases. ... A listing of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ...

Fa

Fab

• Fabry's disease

Fabrys disease (or Angiokeratoma corporis diffusum) is a lysosomal storage disease caused by deficient alpha galactosidase. ...

Fac

Face-Faci

• Faces syndrome
• Facial asymmetry temporal seizures
• Facial clefting corpus callosum agenesis
• Facial dysmorphism macrocephaly myopia Dandy Walker type
• Facial dysmorphism shawl scrotum joint laxity syndrome
• Facial paralysis
• Facies unusual arthrogryposis advanced skeletal malformations
• Facio digito genital syndrome recessive form
• Facio skeletal genital syndrome Rippberger type
• Facio thoraco genital syndrome
• Faciocardiomelic dysplasia lethal
• Faciocardiorenal syndrome
• Faciooculoacousticorenal syndrome
• Facioscapulohumeral muscular dystrophy

Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant form of muscular dystrophy that initially affects muscles of the face (facio), scapula (scapulo) and upper arms (humeral). ...

Fact

• Factor II deficiency
• Factor V deficiency
• Factor V Leiden mutation
• Factor VII deficiency
• Factor VIII deficiency
• Factor X deficiency, congenital
• Factor X deficiency
• Factor XI deficiency, congenital
• Factor XIII deficiency, congenital
• Factor XIII deficiency

Thrombin (activated Factor II) is a coagulation protein that has many effects in the coagulation cascade. ... Factor V is a protein of the coagulation system, rarely referred to as proaccelerin or labile factor. ... Factor V Leiden (sometimes Factor VLeiden) is a hypercoagulability disorder in which Factor V, one of the coagulation factors, cannot be deactivated. ... Factor VII (old name proconvertin) is one of the central proteins in the coagulation cascade. ... Haemophilia A (also spelt Hemophilia A or Hæmophilia A) is a blood clotting disorder caused by a mutation of the Factor VIII gene, leading to a deficiency in Factor VIII. It is the most common hemophilia. ... Factor X, also known by the eponym Stuart-Prower factor or as thrombokinase, is an enzyme (EC 3. ... Factor X, also known by the eponym Stuart-Prower factor or as thrombokinase, is an enzyme (EC 3. ... Factor XI or plasma thromboplastin antecent is one of the enzymes of the coagulation cascade. ... Factor XIII or fibrin stabilizing factor is an enzyme (EC 2. ... Factor XIII or fibrin stabilizing factor is an enzyme (EC 2. ...

Fah-Fal

• Fahr's disease
• Fairbank disease
• Fallot tetralogy

In medicine, the tetralogy of Fallot (described by Etienne Fallot, 1850 - 1911, Marseille) is a significant and complex congenital heart defect, involving four different heart malformations: A ventricular septal defect (VSD), a hole between the two bottom chambers (ventricles) of the heart. ...

Fam

Fami

Famil

Famili

Familial a-Familial i

• Familial adenomatous polyposis
• Familial amyloid polyneuropathy
• Familial aortic dissection
• Familial band heterotopia
• Familial Cold Autoinflamatory Syndrome (FCAS)
• Familial Colorectal Cancer
• Familial deafness
• Familial dilated cardiomyopathy
• Familial emphysema
• Familial hyperchylomicronemia
• Familial hyperlipoproteinemia type I
• Familial hyperlipoproteinemia type III
• Familial hyperlipoproteinemia type IV
• Familial hyperlipoproteinemia
• Familial hypersensitivity pneumonitis
• Familial hypertension
• Familial hypopituitarism
• Familial hypothyroidism
• Familial intestinal polyatresia syndrome

Familial m-Familial w Familial adenomatous polyposis (FAP) is an inherited condition in which numerous polyps form mainly in the epithelium of the large intestine. ...

• Familial Mediterranean fever
• Familial multiple trichodiscomas
• Familial myelofibrosis
• Familial nasal acilia
• Familial non-immune hyperthyroidism
• Familial opposable triphalangeal thumbs duplication
• Familial partial epilepsy with variable focus
• Familial periodic paralysis
• Familial polyposis
• Familial porencephaly
• Familial supernumerary nipples
• Familial symmetric lipomatosis
• Familial Treacher Collins syndrome
• Familial veinous malformations
• Familial ventricular tachycardia
• Familial visceral myopathy
• Familial wilms tumor 2

Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder that affects groups of patients originating from around the Mediterranean Sea (hence its name). ... Familial periodic paralysis is a form of myopathy that are inherited. ... Familial adenomatous polyposis (FAP) is an inherited condition in which numerous polyps form mainly in the epithelium of the large intestine. ...

Fan-Faz

• Fanconi anemia type 1
• Fanconi anemia type 2
• Fanconi anemia type 3
• Fanconi Bickel syndrome
• Fanconi ichthyosis dysmorphism
• Fanconi like syndrome
• Fanconi pancytopenia
• Fanconi syndrome
• Fanconi syndrome, renal, with nephrocalcinosis and renal stones
• Fanconi's anemia
• Fara Chlupackova syndrome
• Farber's disease
• Farmer's lung
• Fas deficiency
• Fascioliasis
• Fatal familial insomnia
• Fatty liver
• Faulk Epstein Jones syndrome
• Faye Petersen Ward Carey syndrome
• Fazio Londe syndrome

Fanconi syndrome (also known as Fanconis syndrome) is a disorder in which the proximal tubular function of the kidney is impaired, resulting in improper reabsorption of electrolytes and nutrients back into the bloodstream. ... Fanconi anemia (FA) is a rare genetic disease that affects children and adults from all ethnic backgrounds. ... Farber disease (also known as Farber’s lipogranulomatosis or ceramidase deficiency) describes a group of rare autosomal recessive disorders that cause an accumulation of fatty material in the joints, tissues and central nervous system. ... Farmers lung is an hypersensitivity pneumonitis induced by the inhalation of biologic dusts coming from moldy hay or other agricultural products. ... Fascioliasis is caused by the trematodes Fasciola hepatica (the sheep liver fluke) and Fasciola gigantica, parasites of herbivores that can infect humans accidentally. ... Fatal familial insomnia (FFI) is a very rare autosomal dominant inherited disease of the brain. ... Fatty liver or steatosis hepatis is a reversible condition seen in chronic alcoholism and many other conditions, where large vacuoles of lipid accumulate in hepatocytes (the cells of the liver). ...

Fe

Fea-Fer

• Fealty syndrome
• Febrile seizure
• Fechtner syndrome
• Feigenbaum Bergeron Richardson syndrome
• Feigenbaum Bergeron syndrome
• Feingold Trainer syndrome
• Felty's Syndrome
• Female pseudohermaphrodism Genuardi type
• Female pseudohermaphrodism
• Femoral facial syndrome
• Femur bifid with monodactylous ectrodactyly
• Femur fibula ulna syndrome
• Fenton Wilkinson Toselano syndrome
• Ferlini Ragno Calzolari syndrome
• Fernhoff Blackston Oakley syndrome
• Ferrocalcinosis cerebro vascular

A febrile seizure, also known as a fever fit or febrile convulsion is a generalized convulsion caused by elevated body temperature. ...

Fet

• Fetal acitretin syndrome
• Fetal akinesia syndrome X linked
• Fetal aminopterin syndrome
• Fetal and neonatal alloimmune thrombocytopenia
• Fetal antihypertensive drugs syndrome
• Fetal brain disruption sequence
• Fetal cytomegalovirus syndrome
• Fetal diethylstilbestrol syndrome
• Fetal edema
• Fetal enterovirus syndrome
• Fetal hydantoin syndrome
• Fetal indomethacin syndrome
• Fetal iodine syndrome
• Fetal left ventricular aneurysm
• Fetal methimazole syndrome
• Fetal methyl mercury syndrome
• Fetal minoxidil syndrome
• Fetal parainfluenza virus type 3 syndrome
• Fetal parvovirus syndrome
• Fetal phenothiazine syndrome
• Fetal prostaglandin syndrome
• Fetal thalidomide syndrome
• Fetal warfarin syndrome

Diethylstilbestrol (DES) is a drug, a synthetic estrogen that was developed to supplement a womans natural estrogen production. ... Phenytoin sodium (marketed as Dilantin® in the USA and as Epanutin® in the UK, by Parke-Davis, now part of Pfizer) is a commonly used antiepileptic. ... Methylmercury (sometimes methyl mercury), an organometallic positive ion (cation), is a widespread bioaccumulative environmental toxin. ... Hydrops fetalis is blood condition in the fetus characterized by an edema in the fetal subcutaneous tissue, sometimes leading to spontaneous abortion. ... It has been suggested that Neurosedyn be merged into this article or section. ... Warfarin (also known under the brand names of Coumadin® and Marevan®) is an anticoagulant medication that is administered orally. ...

Fg

• FG syndrome

Fi

Fib-Fil

• Fiber type disproportion, congenital
• Fibrinogen deficiency, congenital
• Fibrochondrogenesis
• Fibrolipomatosis
• Fibroma
• Fibromatosis gingival hypertrichosis
• Fibromatosis multiple non ossifying
• Fibromatosis
• Fibromuscular dysplasia of arteries
• Fibromuscular dysplasia
• Fibrosarcoma
• Fibrosing alveolitis
• Fibrosing Mediastinitis
• Fibrosis
• Fibrous dysplasia of bone
• Fibrous dysplasia
• Fibrodysplasia ossificans progressiva
• Fibula aplasia complex brachydactyly
• Fibular aplasia ectrodactyly
• Fibular hypoplasia femoral bowing oligodactyly
• Fibular hypoplasia scapulo pelvic dysplasia absent
• Filariasis
• Filippi syndrome

Fibroma. ... Categories: Move to Wiktionary | Medicine stubs ... Fibromuscular dysplasia is a disease that causes renal artery stenosis, which leads to hypertension. ... Fibrosarcoma (fibroblastic sarcoma) is a malignant tumor derived from fibrous connective tissue and characterized by immature proliferating fibroblasts or undifferentiated anaplastic spindle cells. ... Fibrosis is the formation or development of excess fibrous connective tissue in an organ or tissue as a reparative or reactive process, as opposed to formation of fibrous tissue as a normal constituent of an organ or tissue. ... Fibrous Dysplasia is a disease that causes growths or lesions in one or more bones of the human body. ... Fibrodysplasia ossificans progressiva (FOP) is a rare disorder of the connective tissue, in which fibrous tissue (including bone, muscle, tendon, and ligament) is ossified and slowly turned into bone. ...

Fin-Fit

• Fine Lubinsky syndrome
• Fingerprints absence syndactyly milia
• Finnish lethal neonatal metabolic syndrome
• Finnish type amyloidosis
• Finucane Kurtz Scott syndrome
• Fish poisoning
• Fish-eye disease
• Fissured tongue
• Fistulous vegetative verrucous hydradenoma
• Fitz-Hugh-Curtis syndrome
• Fitzsimmons Walson Mellor syndrome
• Fitzsimmons-Guilbert syndrome
• Fitzsimmons-McLachlan-Gilbert syndrome

Fissured tongue is a benign condition characterized by deep grooves (fissures) in dorsum of tongue. ... Fitz-Hugh-Curtis syndrome is a rare complication of pelvic inflammatory disease (PID) named after the two physicians, Fitz-Hugh and Curtis who first reported this condition. ...

Fl

• Flavimonas oryzihabitans
• Flesh eating bacteria
• Floating-harbor syndrome
• Florid cystic endosalpingiosis of the uterus
• Flotch syndrome
• Fluorosis
• Flynn Aird syndrome

Necrotizing fasciitis is a serious but rare infection of the deeper layers of skin and subcutaneous tissues (fascia). ... The word Fluorosis can refer to: Skeletal fluorosis Dental fluorosis This is a disambiguation page — a navigational aid which lists pages that might otherwise share the same title. ... Flynn-Aird Syndrome is a rare, autosomal dominant, hereditary degenerative neurological disorder characterized by early-onset dementia, ataxia, muscle wasting, skin atrophy, and eye abnormalities. ...

Fo

• Focal agyria pachygyria
• Focal alopecia congenital megalencephaly
• Focal dermal hypoplasia
• Focal dystonia
• Focal facial dermal dysplasia
• Focal or multifocal malformations in neuronal migration
• Foix Chavany Marie syndrome
• Foix-Alajouanine syndrome
• Follicular atrophoderma-basal cell carcinoma
• Follicular Dendritic Cell Tumor
• Follicular hamartoma alopecia cystic fibrosis
• Follicular ichthyosis
• Follicular lymphoma
• Follicular lymphoreticuloma
• Fontaine Farriaux Blanckaert syndrome
• Forbes Albright syndrome
• Forbes disease
• Forestier's disease
• Formaldehyde poisoning
• Forney Robinson Pascoe syndrome
• Fountain syndrome
• Fowler Christmas Chapele syndrome
• Fox-Fordyce disease

Focal dystonia is a neurological condition affecting a muscle or muscles in a part of the body causing an undesirable muscular contraction or twisting. ... Foix-Alajouanine syndrome is a disorder caused by an arteriovenous malformation of the spinal cord. ... Follicular lymphoma (FL) is the most common of the indolent non-Hodgkins lymphomas. ... Glycogen storage disease type III is a genetic disorder, an inborn error of metabolism characterized by a deficiency in glycogen debranching enzymes. ... The chemical compound formaldehyde (also known as methanal), is a gas with a pungent smell. ... Fountain syndrome is an autosomal recessive disorder chracterized by mental retardation, deafness, skeletal abnormalities and a coarse face with full lips. ...

Fr

Fra

• Fragile X syndrome type 1
• Fragile X syndrome type 2
• Fragile X syndrome type 3
• Fragile X syndrome
• Fragoso Cid Garcia Hernandez syndrome
• Franceschetti-Klein syndrome
• Francheschini Vardeu Guala syndrome
• Francois dyscephalic syndrome
• Franek Bocker kahlen syndrome
• Fraser Jequier Chen syndrome
• Fraser like syndrome
• Fraser syndrome
• Frasier syndrome
• FRAXA syndrome
• FRAXD
• FRAXE syndrome

Fragile X Syndrome is the most common inherited cause of mental retardation, and is associated with autism. ... An autosomal recessive genetic disease, characterized by developmental defects including underdevelopment of the eyes (crytophthalmos) and the genitals (micropenis, cryptorchidism or clitoromegaly). ... Fragile X Syndrome is the most common inherited cause of mental impairment, and the most common known cause of autism. ...

Fre-Fri

• Free sialic acid storage disease
• Freeman-Sheldon syndrome
• Freiberg's disease
• Freire Maia odontotrichomelic syndrome
• Freire Maia Pinheiro Opitz syndrome
• Frenkel Russe syndrome
• Frey's syndrome
• Frias syndrome
• Fried Goldberg Mundel syndrome
• Friedel Heid Grosshans syndrome
• Friedman Goodman syndrome
• Friedreich ataxia congenital glaucoma
• Friedreich's ataxia
• Frigophobia

Friedreichs ataxia is a rare autosomal recessive disorder caused by a mutation in Gene X25 that codes for frataxin, located on chromosome 9. ...

Fro-Fru

• Froelich's syndrome
• Frölich's syndrome
• Fronto nasal malformation cloacal exstrophy
• Frontofacionasal dysplasia type Al gazali
• Fronto-facio-nasal dysplasia
• Frontometaphyseal dysplasia
• Frontonasal dysplasia acromelic
• Frontonasal dysplasia klippel feil syndrome
• Frontonasal dysplasia phocomelic upper limbs
• Frontonasal dysplasia
• Frontotemporal dementia
• Froster huch syndrome
• Froster Iskenius Waterson syndrome
• Fructose intolerance
• Fructose-1,6-bisphosphatase deficiency
• Fructose-1-phosphate aldolase deficiency, heredita
• Fructosemia, hereditary
• fructosuria

Fronto-temporal dementias selectively affect the frontal lobe of the brain. ... Fructose intolerance is a hereditary condition due to a deficiency of liver enzymes that metabolise fructose. ... Fructose bisphosphatase (EC 3. ...

Fry

• Frydman Cohen Ashenazi syndrome
• Frydman Cohen Karmon syndrome
• Fryer syndrome
• Fryns Fabry Remans syndrome
• Fryns Hofkens Fabry syndrome
• Fryns smeets thiry syndrome

Fu

• Fucosidosis type 1
• Fucosidosis
• Fuhrmann Rieger De sousa syndrome
• Fukuda Miyanomae Nakata syndrome
• Fukuyama type muscular dystrophy
• Fumarase deficiency
• Fumaric aciduria
• Functioning pancreatic endocrine tumor
• Fuqua Berkovitz syndrome
• Furlong Kurczynski Hennessy syndrome
• Furukawa Takagi Nakao syndrome
• Furunculous myiasis
• Fused mandibular incisors