Explore the signs and symptoms, genetic cause, and inheritance pattern of various health conditions.

• 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 1
• Faciopalatoosseous syndrome, see Otopalatodigital syndrome type 2
• 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's disease
• 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 Hailey-Hailey disease
• 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 3, see PLCG2-associated antibody deficiency and immune dysregulation
• Familial cold autoinflammatory syndrome type 2
• Familial cold urticaria with common variable immunodeficiency, see PLCG2-associated antibody deficiency and immune dysregulation
• Familial cold-induced autoinflammatory syndrome type 2, see Familial cold autoinflammatory syndrome type 2
• 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 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 hypercholesterolaemia, see Familial hypercholesterolemia
• Familial hypercholesterolemia
• 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 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 gouty nephropathy, see Autosomal dominant tubulointerstitial kidney disease-UMOD
• Familial juvenile hyperuricemic nephropathy 1, see Autosomal dominant tubulointerstitial kidney disease-UMOD
• 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
• Fatal infantile lactic acidosis with methylmalonic aciduria, see SUCLG1-related mitochondrial DNA depletion syndrome
• 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
• FBS, see Freeman-Sheldon syndrome
• 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
• FCAS2, see Familial cold autoinflammatory syndrome type 2
• FCAS3, see PLCG2-associated antibody deficiency and immune dysregulation
• FCMD, see Fukuyama congenital muscular dystrophy
• FCS syndrome, see Costello 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
• Female-pattern hair loss, see Androgenetic alopecia
• 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
• FGFR1-related osteoglophonic dysplasia, see Osteoglophonic dysplasia
• FGFR3-associated coronal synostosis, see Muenke syndrome
• FGS, see FG syndrome
• FGS1, see FG syndrome
• FH, see Familial hypercholesterolemia
• 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 Autosomal dominant tubulointerstitial kidney disease-UMOD
• FKTN-related congenital muscular dystrophy, see Fukuyama congenital muscular dystrophy
• 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
• FOP, see Fibrodysplasia ossificans progressiva
• 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 1
• FPO, see Otopalatodigital syndrome type 2
• 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 syndrome, see Fragile XE syndrome
• FRDA, see Friedreich ataxia
• Free sialic acid storage disorder
• Freeman-Burian syndrome, see Freeman-Sheldon syndrome
• 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 lobar degeneration
• 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
• FSASD, see Free sialic acid storage disorder
• 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 lobar degeneration
• FTD-PGRN, see GRN-related frontotemporal lobar degeneration
• FTD3, see CHMP2B-related frontotemporal dementia
• FTDP-17, see Frontotemporal dementia with parkinsonism-17
• FTDP-17 GRN, see GRN-related frontotemporal lobar degeneration
• FTDU-17, see GRN-related frontotemporal lobar degeneration
• FTLD, see GRN-related frontotemporal lobar degeneration
• FTLD with TDP-43 pathology, see GRN-related frontotemporal lobar degeneration
• FTLD-TDP, see GRN-related frontotemporal lobar degeneration
• 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
• Fucosidosis
• Fukuhara disease, see Myoclonic epilepsy with ragged-red fibers
• 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