F - diseases

- F13A deficiency - F13B deficiency - Fabry's disease - face blindness - facial (CN VII) palsy - facial agnosia - facial blindness - facial erythema - facial granuloma - facial idiopathic granulomas with regressive evolution - facial nerve disorder - facial pain - facial spasm - facial-oral apraxia - faciobrachial dystonic seizure - faciocutaneoskeletal syndrome - faciodigitogenital syndrome - faciooculoacousticorenal syndrome - facioscapulohumeral dystrophy - facioscapulohumeral muscular dystrophy - factitious hearing loss - factitious hyperthyroidism - factitious thyrotoxicosis - factitious urticaria - factor IX deficiency - factor V autoantibody - factor V deficiency - factor V Quebec - factor VII autoantibody - factor VIII alloAb - factor VIII autoantibody - factor VIII deficiency - factor X autoantibody - factor X deficiency - factor XI deficiency; plasma thromboplastin antecedent deficiency; Rosenthal syndrome - factor XII deficiency - factor XIII deficiency - factor-13-deficiency - factor-5-quebec - FAD APP A692G mutation - FAD APP A692G mutation (FAD1) - Fahr's disease - failed back syndrome - failure to thrive - fainting - falciform ligament sign - fall backward - falling backward - fallopian tube disease - fallopian tube disorder - falls & fractures in the elderly - falls in the elderly - familial ad - familial advanced sleep-phase syndrome - familial alzheimer disease - familial Alzheimer's disease - familial Alzheimer's disease type 1 - familial Alzheimer's disease type 2 - familial Alzheimer's disease type 3 - familial Alzheimer's disease type 4 - familial Alzheimer's disease type 5 - familial Alzheimer's disease [PS2/ASN141ILE] - familial alzheimers disease - familial amyloid polyneuropathy type 3 - familial amyloid polyneuropathy type III - familial amyotrophic lateral sclerosis - familial amyotrophy-dementia-parkinsonism - familial aortic aneurysm - familial arrhythmogenic right ventricular dysplasia - familial arrhythmogenic right ventricular dysplasia 8 - familial arrhythmogenic right ventricular dysplasia type 10 - familial arrhythmogenic right ventricular dysplasia type 11 - familial arrhythmogenic right ventricular dysplasia type 12 - familial arrhythmogenic right ventricular dysplasia type 9 - familial atrial standstill - familial atypical multiple mole melanoma-pancreatic syndrome - familial breast-ovarian cancer - familial British dementia (cerebral amyloid angiopathy ITM2B-related type 1, CAA-ITM2B1) - familial candidiasis type 2 - familial candidiasis type 6 - familial cirrhosis & hepatitis - familial cold autoinflammatory syndrome - familial combined hyperlipidemia - familial combined pituitary hormone deficiency - familial cylindromatosis - familial Danish dementia (cerebral amyloid angiopathy ITM2B-related type 2, CAA-ITM2B2, heredopathia ophthalmo-oto-encephalica) - familial dementia, Neumann type - familial diarrhea type 2 - familial diarrhea type 3 - familial diarrhea type 4 - familial disseminated atypical mycobacterial infection - familial dysalbuminemia - familial dysalbuminemic hyperthyroxinemia - familial dysautonomia - familial dysautonomia type 2 - familial dysbetalipoproteinemia - familial dystonia with visual failure & striatal lucencies - familial encephalopathy with neuroserpin inclusion bodies - familial erythrocytosis - familial erythrocytosis type 1 - familial erythrocytosis type 2 - familial erythrocytosis type 3 - familial erythrophagocytic lymphohistiocytosis - familial expansile osteolysis - familial exudative vitreoretinopathy - familial exudative vitreoretinopathy 4 - familial exudative vitreoretinopathy type 1; autosomal dominant familial exudative vitreoretinopathy - familial exudative vitreoretinopathy type 4 - familial febrile convulsions - familial febrile seizures - familial focal segmental glomerulosclerosis - familial glucocorticoid deficiency - familial glucocorticoid deficiency type-1 - familial granulomatous inflammatory arthritis, dermatitis & uveitis - familial hamartomatous polyposis - familial hemiplegic migraine 2 - familial hemiplegic migraine type 3 - familial hemophagocytic lymphohistiocytosis type 2 - familial hemophagocytic lymphohistiocytosis type 3 - familial hemophagocytic lymphohistiocytosis type 4 - familial hibernian fever - familial histiocytic reticulosis - familial horizontal gaze palsy with progressive scoliosis - familial hyperalphalipoproteinemia - familial hypercholesterolemia - familial hyperchylomicronemia - familial hyperinsulinemic hypoglycemia - familial hyperthyroidism due to inappropriate thyrotropin secretion - familial hypertriglyceridemia - familial hypertrophic cardiomyopathy - familial hypertrophic cardiomyopathy type 1 - familial hypertrophic cardiomyopathy type 4 - familial hypertrophic cardiomyopathy, type 1 - familial hypertrophic cardiomyopathy, type 4 - familial hypoalphalipoproteinemia type 2 - familial hypocalciuric hypercalcemia - familial hypocalciuric hypercalcemia type I - familial hypomagnesemia type 3 - familial hypomagnesemia type 4 - familial hypomagnesemia with hypercalciuria & nephrocalcinosis - familial hypophosphatasia - familial hypoplastic glomerulocystic kidney disease - familial incomplete male pseudohermaphroditism type 2 - familial incontinentia pigmenti - familial incontinentia pigmenti type II - familial infantile myasthenia gravis 2 - familial infiltrative fibromatosis - familial intrahepatic cholestasis 1 - familial intrahepatic cholestasis 2 - familial intrahepatic cholestasis 3 - familial intrahepatic cholestasis 4 - familial isolated hypoparathyroidism - familial isolated vitamin E deficiency - familial juvenile hyperuricemic nephropathy - familial lichen amyloidosis - familial ligand-defective apolipoprotein B-100 - familial lipoma syndrome - familial male precocious puberty - familial Mediterranean fever - familial nephrotic syndrome type-1 - familial neutropenia - familial nonchromaffin paraganglioma - familial nonchromaffin paraganglioma 1 - familial nonchromaffin paraganglioma 3 - familial nonchromaffin paraganglioma 4 - familial nonpolyposis colon cancer - familial nonpolyposis colon cancer type 6 - familial nonpolyposis colon cancer type 7 - familial obesity - familial partial lipodystrophy - familial partial lipodystrophy type 2 - familial periodic paralysis - familial persistent pulmonary hypertension of the newborn - familial platelet disorder with associated myeloid malignancy - familial polymorphic ventricular tachycardia - familial primary pulmonary hypertension - familial progressive hyperpigmentation - familial progressive subcortical gliosis - familial pyrimidinemia - familial rectal pain - familial recurrent arthritis - familial reticuloendotheliosis with eosinophilia - familial scaphocephaly syndrome - familial thoracic aortic aneurysm & dissection - familial tooth agenesis - familial tumoral calcinosis - Fanconi anemia - Fanconi anemia complementation group C - Fanconi anemia complementation group J - fanconi renotubular syndrome - Fanconi syndrome - fanconi's anemia - fanconi's syndrome - Fanconi-Bickel syndrome - fanconis anemia - fanconis syndrome - Farber disease - farmer's lung - FART - fasciculation (muscle twitching) - fasciculation cramp syndrome - fasciitis - Fascioliasis - fat embolism - fat embolism syndrome - fat embolus - fat hypertrophy - fat stranding - fatal ataxia X-linked with deafness & loss of vision - fatal infantile cardioencephalomyopathy with cytochrome c oxidase deficiency - fatal infantile encephalopathy with mitochondrial respiratory chain - fatigue - fatigue fracture - fatty acid delta-6 desaturase deficiency - Fatty degeneration of heart - fatty liver - fatty liver of pregnancy - favism - Favre-Durand-Nicholas disease - Favre-Racouchot syndrome - Fazio-Londe disease - fe deficiency - fear of crowds - febrile - febrile convulsion - febrile granulocytopenia - febrile granulocytopenic patient - febrile mucocutaneous disease - febrile neutropenia - febrile neutropenic patient - febrile seizure - fecal impactation - fecal impaction - fecal incontinence - Fechtner syndrome - feeding disorder - feet pain - Feingold syndrome - felon - felty syndrome - Felty's syndrome - feltys syndrome - female genital mutilation - female infertility - feminization - femoral fracture - femoral head dislocation - femoroacetabular impingement - fenwick hunner ulcer - fertile eunuch syndrome - festinating gait - festination - fetal akinesia deformation sequence - Fetal Alcohol Spectrum Disorder - fetal alcohol syndrome - fetal death - fetal distress - fetal heart rate variability - fetal hydrops - fetal valproate syndrome - fetal valproic acid syndrome - fetishism - fetor oris - Feuerstein & Mims syndrome - fever - fever & rash - fever in a returning traveler - fever in the elderly - Fever of Uncertain Source - fever of unknown origin - Fever without a Source - FG syndrome type 1 - FG syndrome type 4 - fibrillary glomerulonephritis - fibrillinopathy - fibroadenoma - fibrochondrogenesis - fibrocystic disease of the breast - fibrodysplasia ossificans progressiva - fibrofolliculoma - fibrohistiocytic neoplasm - fibroid - fibroleiomyoma - fibromuscular disease - fibromuscular dysplasia - fibromyalgia in the elderly - fibromyalgia syndrome - fibromyositis - fibromyxoid sarcoma - fibrosing colonopathy - fibrosing mediastinitis - fibrosis - fibrositis - fibrotic interstitial lung disease - fibrous adenosis - fibrous adhesion - fibrous dysplasia - fibrous mesothelioma - fibrous tissue neoplasm - fibroxanthoma - fibular aplasia or hypoplasia femoral bowing & poly- syn- & oligodactyly - fibular fracture - fibular hypoplasia & complex brachydactyly - fibular neuropathy - ficolin-3 deficiency - fifth digit syndrome - fifth disease - figurate dermatitis - filariasis - finger tip bluish tint - finger tip cyanosis - fingernail pitting - finkelstein sign - Finkelstein's sign - finkelsteins sign - finnish congenital nephropathy - Finnish congenital nephrosis - Finnish type amyloidosis - Finnish type congenital nephropathy - Finnish variant late infantile neuronal ceroid lipofuscinosis - Finnish-type congenital nephropathy - first carpometacarpal joint osteoarthritis - first carpometacarpal joint osteoarthritis - first degree atrioventricular block - first degree AV block - first degree burn - first degree heart block - first disease - first heart sound (S1) - first metatarsophalangeal joint osteoarthritis - first-degree atrioventricular (AV) block - fish-odor syndrome - Fisher syndrome - fissure in ano - fistula-in-ano - Fitz Hugh Curtis syndrome - Fitz-Hugh-Curtis syndrome - fixed drug eruption - flaccid bullae - flaccid paralysis - flacid paralysis - flagellin (CBir) antibody - flail chest - flame-shaped splinter hemorrhage - flank pain - flashes - flashing lights - flat adenoma syndrome - flat feet - flat foot - flat wart - flatbush diabetes mellitus - flatfoot - flatulence - flatus - floater - floating kidney - FLU - fluent aphasia (Wernicke's aphasia) - fluid imbalance - fluid retention - fluoride poisoning - fluoride toxicity - fluorosis - flushing - flutter - Flynn-Aird syndrome - FMD - FMF - foamy urine - focal cortical dysplasia - focal cortical dysplasia of Taylor balloon cell type - focal dermal hypoplasia - focal dystonia - focal epilepsy - focal glomerular sclerosis - focal glomerulonephritis - focal glomerulosclerosis - focal motor aware seizure - focal motor seizure - focal neurologic defect - focal neurologic deficit - focal neurologic sign - focal neurological deficit - focal neurological sign - focal nodular hyperplasia - focal segmental glomerular sclerosis - focal segmental glomerulosclerosis - focal segmental glomerulosclerosis type 1 - focal segmental glomerulosclerosis type 2 - focal segmental glomerulosclerosis type 3 - focal segmental glomerulosclerosis type 4 - focal segmental glomerulosclerosis type 6 - focal seizure - focal seizure with impaired awareness - folate deficiency - folate-sensitive fragile site FRA10A expression - folic acid deficiency - folicular B-cell lymphoma - follicle center lymphoma, grade I - follicle center lymphoma, grade II - follicle center lymphoma, grade III - follicuar lymphoma grade 1 - follicuar lymphoma grade 2 - follicular hyperkeratosis - follicular keratosis - follicular large cell lymphoma - follicular lichen planus - follicular mixed small & large cell lymphoma - follicular occlusion syndrome - follicular small cleaved cell lymphoma - follicular thyroid adenoma - follicular thyroid carcinoma - folliculitis - folliculitis keloidalis - food allergy - food hypersensitivity - food insecurity - food poisoning - food sensitivity - food sensitization from allergy - foodborne bioterrorism - foodborne disease - foodborne illness - foot deformity - foot drop - foot ischemia - foot pain - foot slap - foramina parietalia permagna - Forchheimer sign - fordyce disease - fordyce granule - Fordyce spot (granule) - fordyce's disease - fordyce's spot - fordyces disease - fordyces spot - forefoot pain - foreign body aspiration - Foreign Body of External Eye - foreign body of eye - foreign body of the eye - foreign body sensation (eye) - forgetting - formiminoglutamicaciduria - Forsius-Eriksson type ocular albinism - Foster-Kennedy syndrome - fournier gangrene - Fournier's gangrene - fourniers gangrene - fourth degree burn - fourth disease - fourth heart sound (S4) - foveal hypoplasia - fracture - fracture of femur - fracture of fibula - fracture of pelvis - fracture of penis - fracture of radius - Fracture Of Rib(s) - fracture of sternum - fracture of the cervical spine - fracture of the femur - fracture of the hip - fracture of the penis - fracture of the plevis - fracture of the proximal humerus - fracture of the sternum - fracture, cervical spine - fragile X syndrome - fragile X syndrome FRAXA site - fragile X syndrome FRAXE site - fragile X tremor/ataxia syndrome - fragilitas ossium - fragility fracture - frailness - frailty - frambesia - Fraser syndrome - Frasier syndrome - freckle - free-floating anxiety - Freeman-Sheldon syndrome - freezing gait - freezing of gait - freidreich ataxia - freidreich's ataxia - freidreichs ataxia - freidrich ataxia - freidrich's ataxia - freidrichs ataxia - fremitus - frequency of micturition - frequent urination - frey baillarger syndrome - frey syndrome - frey's syndrome - freys syndrome - friable cervix - friction blister - friction fremitus - friction rub - frictional blister - friderichsen waterhouse syndrome - Friedreich ataxia - friedreich's ataxia - friedreichs ataxia - friedrich ataxia - friedrich's ataxia - friedrichs ataxia - fright neurosis - Frommel disease - frontal dementia - frontal fibrosing alopecia - frontal lobe syndrome - frontal-subcortical dementia - frontometaphyseal dysplasia - frontonasal dysplasia - frontonasal malformation - frontorhiny - frontotemporal degeneration - frontotemporal dementia - frontotemporal dementia 3 - frontotemporal dementia with parkinsonism - frontotemporal lobe dementia - frontotemporal neurocognitive disorder - frotteurism - frozen shoulder - fructose intolerance - fructose-1,6-diphosphatase deficiency - FSGS - FSHD - FTD - FTD3 - FTDP-17 - FTLD - fuch dystrophy - fuch's dystrophy - Fuchs' dystrophy - fucosidosis - Fuhrmann syndrome - Fukuyama congenital muscular dystrophy - Fukuyama type congenital muscular dystrophy - fuliminant hepatic failure - fulminant hepatitic failure - fulminant hepatitis - fulminant liver failure - fumarase deficiency - fumaric aciduria - functional cognitive disorder - functional dyspepsia - functional incontinence - functional neurologic symptom disorder - functional urinary incontinence - fundic gland polyp - fundus albipunctatus - fundus flavimaculatus - fungal arthritis - fungal bladder infection - fungal cystitis - fungal infection - fungal meningitis - fungal pneumonia - fungus ball - Furlong syndrome - furuncle - furuncular - furunculosis - fusospirochetosis - futcher line