Genetic diseases-F
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- F10 deficiency see Factor X deficiency
- F11 deficiency see Factor XI deficiency
- F7 deficiency see Factor VII deficiency
- FA see Fanconi anemia
- FA see Friedreich ataxia
- FAA see Familial thoracic aortic aneurysm and dissection
- Fabry disease
- Fabry's disease see Fabry disease
- facio-digito-genital dysplasia see Aarskog-Scott syndrome
- Facio-genito-popliteal syndrome see Popliteal pterygium syndrome
- facio-scapulo-humeral dystrophy see Facioscapulohumeral muscular dystrophy
- facioauriculovertebral dysplasia see Craniofacial microsomia
- faciocutaneoskeletal syndrome see Costello syndrome
- faciodigitogenital syndrome see Aarskog-Scott syndrome
- faciogenital dysplasia see Aarskog-Scott syndrome
- faciooculoacousticorenal syndrome see Donnai-Barrow syndrome
- faciopalatoosseous syndrome see Otopalatodigital syndrome type 2
- faciopalatoosseous syndrome see Otopalatodigital syndrome type 1
- facioscapulohumeral atrophy see Facioscapulohumeral muscular dystrophy
- Facioscapulohumeral muscular dystrophy
- facioscapulohumeral type progressive muscular dystrophy see Facioscapulohumeral muscular dystrophy
- facioscapuloperoneal muscular dystrophy see Facioscapulohumeral muscular dystrophy
- factor 11 deficiency see Factor XI deficiency
- factor II deficiency see Prothrombin deficiency
- Factor V deficiency
- Factor V Leiden thrombophilia
- Factor VII deficiency
- Factor X deficiency
- Factor XI deficiency
- Factor XIII deficiency
- FACU see PLCG2-associated antibody deficiency and immune dysregulation
- FAHN see Fatty acid hydroxylase-associated neurodegeneration
- Fairbank-Keats syndrome see Osteoglophonic dysplasia
- FALDH deficiency see Sjögren-Larsson syndrome
- familial acoustic neuromas see Neurofibromatosis type 2
- familial acute myeloid leukaemia see Familial acute myeloid leukemia with mutated CEBPA
- Familial acute myeloid leukemia with mutated CEBPA
- Familial adenomatous polyposis
- familial afibrinogenemia see Congenital afibrinogenemia
- familial Alzheimer disease (FAD) see Alzheimer disease
- familial amyloid nephropathy with urticaria and deafness see Muckle-Wells syndrome
- familial amyloid polyneuropathy type IV see Lattice corneal dystrophy type II
- familial amyloidosis, Finnish type see Lattice corneal dystrophy type II
- familial aortic aneurysm see Familial thoracic aortic aneurysm and dissection
- familial aortic dissection see Familial thoracic aortic aneurysm and dissection
- familial aplasia of the vermis see Joubert syndrome
- familial apoceruloplasmin deficiency see Aceruloplasminemia
- familial asymmetric septal hypertrophy see Familial hypertrophic cardiomyopathy
- Familial atrial fibrillation
- familial atypical cold urticaria see PLCG2-associated antibody deficiency and immune dysregulation
- familial benign chronic pemphigus see Benign chronic pemphigus
- Familial benign giant-cell tumor of the jaw see Cherubism
- familial brachial plexus neuritis see Hereditary neuralgic amyotrophy
- Familial candidiasis
- familial cavernous hemangioma see Cerebral cavernous malformation
- familial cavernous malformation see Cerebral cavernous malformation
- familial cerebral cavernous angioma see Cerebral cavernous malformation
- familial cerebral cavernous malformation see Cerebral cavernous malformation
- familial chronic mucocutaneous candidiasis see Familial candidiasis
- Familial cold autoinflammatory syndrome
- familial cold autoinflammatory syndrome 3 see PLCG2-associated antibody deficiency and immune dysregulation
- familial cold urticaria see Familial cold autoinflammatory syndrome
- familial cold urticaria with common variable immunodeficiency see PLCG2-associated antibody deficiency and immune dysregulation
- familial cold-induced autoinflammatory syndrome see Familial cold autoinflammatory syndrome
- Familial cylindromatosis
- familial cystic parathyroid adenomatosis see Hyperparathyroidism-jaw tumor syndrome
- familial dementia with neuroserpin inclusion bodies see Familial encephalopathy with neuroserpin inclusion bodies
- familial diffuse gastric cancer see Hereditary diffuse gastric cancer
- Familial dilated cardiomyopathy
- Familial dysautonomia
- familial dyskinesia with facial myokymia see ADCY5-related dyskinesia
- Familial encephalopathy with neuroserpin inclusion bodies
- familial endocrine adenomatosis see Multiple endocrine neoplasia
- Familial erythrocytosis
- familial erythromelalgia see Erythromelalgia
- familial erythrophagocytic lymphohistiocytosis see Familial hemophagocytic lymphohistiocytosis
- familial exostoses see Hereditary multiple osteochondromas
- Familial exudative vitreoretinopathy
- familial fat-induced hypertriglyceridemia see Familial lipoprotein lipase deficiency
- familial fatal Epstein-Barr infection see X-linked lymphoproliferative disease
- Familial fibrous dysplasia of jaw see Cherubism
- Familial focal epilepsy with variable foci
- familial glomerular nephritis with fibronectin deposits see Fibronectin glomerulopathy
- Familial glucocorticoid deficiency
- familial gonadotrophin-independent sexual precocity see Familial male-limited precocious puberty
- Familial gout-kidney disease see Uromodulin-associated kidney disease
- Familial gouty nephropathy see Uromodulin-associated kidney disease
- familial granulomatosis, Blau type see Blau syndrome
- familial gynecomastia due to increased aromatase activity see Aromatase excess syndrome
- Familial HDL deficiency
- Familial hemiplegic migraine
- familial hemochromatosis see Hereditary hemochromatosis
- familial hemophagocytic histiocytosis see Familial hemophagocytic lymphohistiocytosis
- familial hemophagocytic lymphocytosis see Familial hemophagocytic lymphohistiocytosis
- Familial hemophagocytic lymphohistiocytosis
- familial hemophagocytic reticulosis see Familial hemophagocytic lymphohistiocytosis
- familial Hibernian fever see Tumor necrosis factor receptor-associated periodic syndrome
- Familial High Density Lipoprotein Deficiency Disease see Tangier disease
- familial horizontal gaze palsy with progressive scoliosis see Horizontal gaze palsy with progressive scoliosis
- Familial hyperaldosteronism
- familial hypercalciuric hypocalcemia see Autosomal dominant hypocalcemia
- familial hyperchylomicronemia see Familial lipoprotein lipase deficiency
- familial hyperekplexia see Hereditary hyperekplexia
- familial hyperkalemic hypertension see Pseudohypoaldosteronism type 2
- familial hyperkalemic periodic paralysis see Hyperkalemic periodic paralysis
- familial hyperlysinemia see Hyperlysinemia
- familial hyperpotassemia and hypertension see Pseudohypoaldosteronism type 2
- familial hyperreninemic hypoaldosteronism see Corticosterone methyloxidase deficiency
- familial hypertensive hyperkalemia see Pseudohypoaldosteronism type 2
- Familial hypertrophic cardiomyopathy
- Familial Hypoalphalipoproteinemia see Tangier disease
- familial hypoalphalipoproteinemia see Familial HDL deficiency
- Familial hypobetalipoproteinemia
- familial hypocalcemia see Autosomal dominant hypocalcemia
- familial hypokalemia-hypomagnesemia see Gitelman syndrome
- Familial Hypokalemic Periodic Paralysis see Hypokalemic periodic paralysis
- familial idiopathic basal ganglia calcification see Primary familial brain calcification
- familial idiopathic cardiomyopathy see Familial dilated cardiomyopathy
- familial idiopathic hyperphosphatasemia see Juvenile Paget disease
- familial idiopathic scoliosis associated with congenital encephalopathy see Horizontal gaze palsy with progressive scoliosis
- familial incomplete male pseudohermaphroditism, type 2 see 5-alpha reductase deficiency
- familial infantile encephalopathy with intracranial calcification and chronic cerebrospinal fluid lymphocytosis see Aicardi-Goutières syndrome
- familial infantile scoliosis associated with bilateral paralysis of conjugate gaze see Horizontal gaze palsy with progressive scoliosis
- familial infiltrative fibromatosis see Desmoid tumor
- Familial isolated hyperparathyroidism
- Familial isolated pituitary adenoma
- familial isolated vitamin E deficiency see Ataxia with vitamin E deficiency
- Familial juvenile hyperuricemic nephropathy see Uromodulin-associated kidney disease
- Familial juvenile hyperuricemic nephropathy 2 see REN-related kidney disease
- familial juvenile systemic granulomatosis see Blau syndrome
- familial LCAT deficiency see Complete LCAT deficiency
- familial lecithin-cholesterol acyltransferase deficiency see Complete LCAT deficiency
- Familial lipoprotein lipase deficiency
- familial lobular glomerulopathy see Fibronectin glomerulopathy
- familial LPL deficiency see Familial lipoprotein lipase deficiency
- Familial male-limited precocious puberty
- familial manganese-induced neurotoxicity see Hypermanganesemia with dystonia
- Familial Mediterranean fever
- Familial multilocular cystic disease of the jaws see Cherubism
- familial multiple polyposis syndrome see Familial adenomatous polyposis
- familial multiple trichoepitheliomata see Multiple familial trichoepithelioma
- familial myoclonus with renal failure see Action myoclonus–renal failure syndrome
- familial nephrotic syndrome see Congenital nephrotic syndrome
- familial nodular heterotopia see Periventricular heterotopia
- familial nonhemolytic jaundice see Gilbert syndrome
- familial nonhemolytic unconjugated hyperbilirubinemia see Crigler-Najjar syndrome
- familial nonpolyposis colon cancer see Lynch syndrome
- Familial osteochondritis dissecans
- familial osteodysplasia see Hajdu-Cheney syndrome
- familial osteoectasia see Juvenile Paget disease
- familial palmar fibromatosis see Dupuytren contracture
- familial pancreatitis see Hereditary pancreatitis
- familial paraganglioma syndrome see Hereditary paraganglioma-pheochromocytoma
- familial paraganglioma-pheochromocytoma syndromes see Hereditary paraganglioma-pheochromocytoma
- familial paroxysmal choreoathetosis see Familial paroxysmal nonkinesigenic dyskinesia
- familial paroxysmal dystonia see Familial paroxysmal kinesigenic dyskinesia
- Familial paroxysmal kinesigenic dyskinesia
- Familial paroxysmal nonkinesigenic dyskinesia
- familial paroxysmal polyserositis see Familial Mediterranean fever
- familial partial epilepsy with variable foci see Familial focal epilepsy with variable foci
- Familial partial lipodystrophy
- familial persistent pulmonary hypertension of the newborn see Alveolar capillary dysplasia with misalignment of pulmonary veins
- familial Pick's disease see Frontotemporal dementia with parkinsonism-17
- Familial pityriasis rubra pilaris
- familial polycythemia see Familial erythrocytosis
- familial polymorphic ventricular tachycardia see Catecholaminergic polymorphic ventricular tachycardia
- Familial porencephaly
- familial posterior fossa brain tumor of infancy see Rhabdoid tumor predisposition syndrome
- familial posterior fossa brain tumor syndrome see Rhabdoid tumor predisposition syndrome
- familial pressure sensitive neuropathy see Hereditary neuropathy with liability to pressure palsies
- familial primary aldosteronism see Familial hyperaldosteronism
- familial primary hyperparathyroidism with multiple ossifying jaw fibromas see Hyperparathyroidism-jaw tumor syndrome
- familial primary hypomagnesemia with hypocalcuria see Hypomagnesemia with secondary hypocalcemia
- familial primary pulmonary hypertension see Pulmonary arterial hypertension
- familial progressive scleroderma see Systemic scleroderma
- familial protracted enteropathy see Microvillus inclusion disease
- familial PRP see Familial pityriasis rubra pilaris
- familial pterygium syndrome see Multiple pterygium syndrome
- familial pyrimidemia see Dihydropyrimidine dehydrogenase deficiency
- familial rectal pain see Paroxysmal extreme pain disorder
- familial recurrent hydatidiform mole see Recurrent hydatidiform mole
- familial renal hypouricaemia see Renal hypouricemia
- familial renal hypouricemia see Renal hypouricemia
- Familial restrictive cardiomyopathy
- familial reticuloendotheliosis see Omenn syndrome
- familial retinal arterial macroaneurysm see Retinal arterial macroaneurysm with supravalvular pulmonic stenosis
- familial rhabdoid tumor see Rhabdoid tumor predisposition syndrome
- familial TAAD see Familial thoracic aortic aneurysm and dissection
- familial thoracic aortic aneurysm see Familial thoracic aortic aneurysm and dissection
- Familial thoracic aortic aneurysm and dissection
- Familial Thrombotic Thrombocytopenia Purpura see Thrombotic thrombocytopenic purpura
- familial tremor see Essential tremor
- familial Turner syndrome see Noonan syndrome
- familial vascular leukoencephalopathy see Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- familial veno-occlusive disease with immunodeficiency see Hepatic veno-occlusive disease with immunodeficiency
- familial visceral myopathy see Intestinal pseudo-obstruction
- familial visceral neuropathy see Intestinal pseudo-obstruction
- familial visceral xanthomatosis see Lysosomal acid lipase deficiency
- familial white folded mucosal dysplasia see White sponge nevus
- familial xanthomatosis see Lysosomal acid lipase deficiency
- familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertension see Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Fanconi anemia
- Fanconi hypoplastic anemia see Fanconi anemia
- Fanconi pancytopenia see Fanconi anemia
- Fanconi panmyelopathy see Fanconi anemia
- FAP see Familial adenomatous polyposis
- far-sightedness see Farsightedness
- Farber disease see Farber lipogranulomatosis
- Farber lipogranulomatosis
- Farber's disease see Farber lipogranulomatosis
- Farber's lipogranulomatosis see Farber lipogranulomatosis
- Farber-Uzman syndrome see Farber lipogranulomatosis
- farsighted see Farsightedness
- Farsightedness
- Fatty acid hydroxylase-associated neurodegeneration
- fatty aldehyde dehydrogenase deficiency see Sjögren-Larsson syndrome
- fatty liver see Non-alcoholic fatty liver disease
- FAV see Craniofacial microsomia
- Fazio-Londe disease see Riboflavin transporter deficiency neuronopathy
- Fazio-Londe syndrome see Riboflavin transporter deficiency neuronopathy
- FBCG1 see Fibrochondrogenesis
- FBCG2 see Fibrochondrogenesis
- FBXL4 deficiency see FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome
- FBXL4-related early onset mitochondrial encephalopathy see FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome
- FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome
- FCAS see Familial cold autoinflammatory syndrome
- FCAS3 see PLCG2-associated antibody deficiency and immune dysregulation
- FCMD see Fukuyama congenital muscular dystrophy
- FCS syndrome see Costello syndrome
- FCU see Familial cold autoinflammatory syndrome
- FD see Familial dysautonomia
- FDC see Familial dilated cardiomyopathy
- FDFM see ADCY5-related dyskinesia
- FDGC see Hereditary diffuse gastric cancer
- FED see Fish-eye disease
- Feingold syndrome
- FEL see Familial hemophagocytic lymphohistiocytosis
- Fellman syndrome see GRACILE syndrome
- female pattern baldness see Androgenetic alopecia
- female pseudo-Turner syndrome see Noonan syndrome
- fenestrae parietals symmetricae see Enlarged parietal foramina
- FENIB see Familial encephalopathy with neuroserpin inclusion bodies
- ferritin-related neurodegeneration see Neuroferritinopathy
- FESD see Epilepsy-aphasia spectrum
- fetal face syndrome see Robinow syndrome
- Fetal iritis syndrome see Norrie disease
- fetal myocardium see Left ventricular noncompaction
- FEVR see Familial exudative vitreoretinopathy
- FFEVF see Familial focal epilepsy with variable foci
- FG syndrome
- FGDY see Aarskog-Scott syndrome
- FGFR3-associated coronal synostosis see Muenke syndrome
- FGS see FG syndrome
- FGS1 see FG syndrome
- FH see Familial hyperaldosteronism
- FHA see Familial HDL deficiency
- FHBL see Familial hypobetalipoproteinemia
- FHHt see Pseudohypoaldosteronism type 2
- FHL see Familial hemophagocytic lymphohistiocytosis
- FHLH see Familial hemophagocytic lymphohistiocytosis
- FHS see Floating-Harbor syndrome
- FIBGC see Primary familial brain calcification
- fibrin stabilizing factor deficiency see Factor XIII deficiency
- fibrinoid degeneration of astrocytes see Alexander disease
- Fibrochondrogenesis
- fibrochondrogenesis-1 see Fibrochondrogenesis
- fibrochondrogenesis-2 see Fibrochondrogenesis
- fibrocystic disease of pancreas see Cystic fibrosis
- Fibrodysplasia ossificans progressiva
- fibrofolliculomas with trichodiscomas and acrochordons see Birt-Hogg-Dubé syndrome
- Fibromyalgia
- fibromyalgia syndrome see Fibromyalgia
- fibromyalgia-fibromyositis syndrome see Fibromyalgia
- fibromyositis see Fibromyalgia
- Fibronectin glomerulopathy
- fibrositis see Fibromyalgia
- fibrous dysplasia with pigmentary skin changes and precocious puberty see McCune-Albright syndrome
- FIC1 deficiency see Progressive familial intrahepatic cholestasis
- fifth digit syndrome see Coffin-Siris syndrome
- FIGLU-uria see Glutamate formiminotransferase deficiency
- FIHP see Familial isolated hyperparathyroidism
- filamin-A-associated myxomatous mitral valve disease see X-linked cardiac valvular dysplasia
- filamin-A-related myxomatous mitral valve dystrophy see X-linked cardiac valvular dysplasia
- Finlay-Marks syndrome see Scalp-ear-nipple syndrome
- Finnish lactic acidosis with hepatic hemosiderosis see GRACILE syndrome
- Finnish lethal neonatal metabolic syndrome see GRACILE syndrome
- Finnish variant late infantile neuronal ceroid lipofuscinosis see CLN5 disease
- Finnish vLINCL see CLN5 disease
- FIPA see Familial isolated pituitary adenoma
- first and second branchial arch syndrome see Craniofacial microsomia
- first and second pharyngeal arch syndromes see Craniofacial microsomia
- fish malodor syndrome see Trimethylaminuria
- fish odor syndrome see Trimethylaminuria
- Fish-eye disease
- Fisher syndrome see Guillain-Barré syndrome
- Fishman syndrome (formerly) see Encephalocraniocutaneous lipomatosis
- FIVE see Ataxia with vitamin E deficiency
- FJHN see Uromodulin-associated kidney disease
- FLD see Complete LCAT deficiency
- Fletcher factor deficiency see Prekallikrein deficiency
- Fletcher trait see Prekallikrein deficiency
- FLHS see Floating-Harbor syndrome
- Floating-Harbor syndrome
- flowing hyperostosis see Melorheostosis
- FMD see Frontometaphyseal dysplasia
- FMF see Familial Mediterranean fever
- FMR1-related primary ovarian insufficiency see Fragile X-associated primary ovarian insufficiency
- FMS see Fibromyalgia
- FND see Frontonasal dysplasia
- FNM see Frontonasal dysplasia
- FOAR syndrome see Donnai-Barrow syndrome
- Focal dermal hypoplasia
- focal epilepsies with speech and language disorders see Epilepsy-aphasia spectrum
- focal epilepsy with speech disorder and with or without mental retardation see Epilepsy-aphasia spectrum
- focal hand dystonia see Task-specific focal dystonia
- focal task-specific dystonia see Task-specific focal dystonia
- fOCD see Familial osteochondritis dissecans
- Folic acid transport defect see Hereditary folate malabsorption
- Folling disease see Phenylketonuria
- Folling's disease see Phenylketonuria
- FOLR1 deficiency see Cerebral folate transport deficiency
- Fong disease see Nail-patella syndrome
- foramina parietalia permagna see Enlarged parietal foramina
- Forbes disease see Glycogen storage disease type III
- formiminoglutamic aciduria see Glutamate formiminotransferase deficiency
- formiminotransferase deficiency see Glutamate formiminotransferase deficiency
- FOXG1 syndrome
- FOXG1-related disorder see FOXG1 syndrome
- FOXP2-related speech and language disorder
- FPF see Tumor necrosis factor receptor-associated periodic syndrome
- FPGL see Hereditary paraganglioma-pheochromocytoma
- FPGL/PHEO see Hereditary paraganglioma-pheochromocytoma
- FPL see Familial partial lipodystrophy
- FPO see Otopalatodigital syndrome type 2
- FPO see Otopalatodigital syndrome type 1
- FPP see Enlarged parietal foramina
- FPPH see Pulmonary arterial hypertension
- FPVT see Catecholaminergic polymorphic ventricular tachycardia
- fra(X) syndrome see Fragile X syndrome
- Fragile X syndrome
- fragile X tremor/ataxia syndrome see Fragile X-associated tremor/ataxia syndrome
- Fragile X-associated primary ovarian insufficiency
- Fragile X-associated tremor/ataxia syndrome
- Fragile XE syndrome
- Fragilitas ossium see Osteogenesis imperfecta
- FRAM see Retinal arterial macroaneurysm with supravalvular pulmonic stenosis
- Franceschetti-Jadassohn syndrome see Naegeli-Franceschetti-Jadassohn syndrome/dermatopathia pigmentosa reticularis
- Franceschetti-Zwahlen-Klein syndrome see Treacher Collins syndrome
- Fraser syndrome
- Fraser's syndrome see Fraser syndrome
- Fraser-Francois syndrome see Fraser syndrome
- Frasier syndrome
- FRAXA syndrome see Fragile X syndrome
- FRAXE intellectual deficit see Fragile XE syndrome
- FRAXE intellectual disability see Fragile XE syndrome
- FRAXE mental retardation syndrome see Fragile XE syndrome
- FRAXE syndrome see Fragile XE syndrome
- FRDA see Friedreich ataxia
- free sialic acid storage disease see Sialic acid storage disease
- Freeman-Sheldon syndrome
- French type sialuria see Sialuria
- FRHM see Recurrent hydatidiform mole
- Friedreich ataxia
- Friedreich ataxia phenotype with selective vitamin E deficiency see Ataxia with vitamin E deficiency
- Friedreich spinocerebellar ataxia see Friedreich ataxia
- Friedreich-like ataxia see Ataxia with vitamin E deficiency
- Friedrich's ataxia see Friedreich ataxia
- FRMD7-related infantile nystagmus see X-linked infantile nystagmus
- Frontometaphyseal dysplasia
- Frontonasal dysplasia
- frontonasal dysplasia sequence see Frontonasal dysplasia
- frontonasal malformation see Frontonasal dysplasia
- frontorhiny see Frontonasal dysplasia
- Frontotemporal dementia with parkinsonism-17
- frontotemporal lobar degeneration see GRN-related frontotemporal dementia
- fructose aldolase B deficiency see Hereditary fructose intolerance
- fructose intolerance see Hereditary fructose intolerance
- fructose-1,6-biphosphate aldolase deficiency see Hereditary fructose intolerance
- fructose-1-phosphate aldolase deficiency see Hereditary fructose intolerance
- fructosemia see Hereditary fructose intolerance
- Fryns syndrome
- Fryns-Aftimos syndrome see Baraitser-Winter syndrome
- FS see Frasier syndrome
- FSH muscular dystrophy see Facioscapulohumeral muscular dystrophy
- FSHD see Facioscapulohumeral muscular dystrophy
- FSS see Freeman-Sheldon syndrome
- FTAAD see Familial thoracic aortic aneurysm and dissection
- FTD-3 see CHMP2B-related frontotemporal dementia
- FTD-CHMP2B see CHMP2B-related frontotemporal dementia
- FTD-GRN see GRN-related frontotemporal dementia
- FTD-PGRN see GRN-related frontotemporal dementia
- FTD3 see CHMP2B-related frontotemporal dementia
- FTDP-17 see Frontotemporal dementia with parkinsonism-17
- FTDP-17 GRN see GRN-related frontotemporal dementia
- FTDU-17 see GRN-related frontotemporal dementia
- FTLD see GRN-related frontotemporal dementia
- FTLD with TDP-43 pathology see GRN-related frontotemporal dementia
- FTLD-TDP see GRN-related frontotemporal dementia
- FTSD see Task-specific focal dystonia
- Fuchs atrophy see Fuchs endothelial dystrophy
- Fuchs corneal dystrophy see Fuchs endothelial dystrophy
- Fuchs dystrophy see Fuchs endothelial dystrophy
- Fuchs endothelial corneal dystrophy see Fuchs endothelial dystrophy
- Fuchs endothelial dystrophy
- Fuchs' endothelial dystrophy see Fuchs endothelial dystrophy
- Fucosidase deficiency see Fucosidosis
- Fucosidase Deficiency Disease see Fucosidosis
- Fucosidosis
- Fukuhara Disease see Myoclonic epilepsy with ragged-red fibers
- Fukuyama CMD see Fukuyama congenital muscular dystrophy
- Fukuyama congenital muscular dystrophy
- Fukuyama muscular dystrophy see Fukuyama congenital muscular dystrophy
- Fukuyama syndrome see Fukuyama congenital muscular dystrophy
- Fukuyama type congenital muscular dystrophy see Fukuyama congenital muscular dystrophy
- Fumarase deficiency
- fumarate hydratase deficiency see Fumarase deficiency
- fumaric aciduria see Fumarase deficiency
- Fundus albipunctatus
- fusion of cervical vertebrae see Klippel-Feil syndrome
- FXPOI see Fragile X-associated primary ovarian insufficiency
- FXS see Fragile X syndrome
- FXTAS see Fragile X-associated tremor/ataxia syndrome
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Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.Contributors: Prab R. Tumpati, MD