Genetic diseases-F

• 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