F - diseases
Jump to navigation
Jump to search
Introduction
- 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