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 Familial HDL deficiency
- Familial hypoalphalipoproteinemia, see Tangier disease
- 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