List of diseases (F)
Fa
Fab
Fac
Face-Faci
- Faces syndrome
- Facial asymmetry temporal seizures
- Facial clefting corpus callosum agenesis
- Facial dysmorphism macrocephaly myopia Dandy Walker type
- Facial dysmorphism shawl scrotum joint laxity syndrome
- Facial paralysis
- Facies unusual arthrogryposis advanced skeletal malformations
- Facio digito genital syndrome recessive form
- Facio skeletal genital syndrome Rippberger type
- Facio thoraco genital syndrome
- Faciocardiomelic dysplasia lethal
- Faciocardiorenal syndrome
- Faciooculoacousticorenal syndrome
- Facioscapulohumeral muscular dystrophy
Fact
- Factor II deficiency
- Factor V deficiency
- Factor V Leiden mutation
- Factor VII deficiency
- Factor VIII deficiency
- Factor X deficiency, congenital
- Factor X deficiency
- Factor XI deficiency, congenital
- Factor XIII deficiency, congenital
- Factor XIII deficiency
Fah-Fal
Fam
Fami
Famil
Famili
Familial a-Familial i
- Familial adenomatous polyposis
- Familial amyloid polyneuropathy
- Familial aortic dissection
- Familial band heterotopia
- Familial Cold Autoinflamatory Syndrome (FCAS)
- Familial Colorectal Cancer
- Familial deafness
- Familial dilated cardiomyopathy
- Familial emphysema
- Familial hyperchylomicronemia
- Familial hyperlipoproteinemia type I
- Familial hyperlipoproteinemia type III
- Familial hyperlipoproteinemia type IV
- Familial hyperlipoproteinemia
- Familial hypersensitivity pneumonitis
- Familial hypertension
- Familial hypopituitarism
- Familial hypothyroidism
- Familial intestinal polyatresia syndrome
Familial m-Familial w
- Familial Mediterranean fever
- Familial multiple trichodiscomas
- Familial myelofibrosis
- Familial nasal acilia
- Familial non-immune hyperthyroidism
- Familial opposable triphalangeal thumbs duplication
- Familial partial epilepsy with variable focus
- Familial periodic paralysis
- Familial polyposis
- Familial porencephaly
- Familial supernumerary nipples
- Familial symmetric lipomatosis
- Familial Treacher Collins syndrome
- Familial veinous malformations
- Familial ventricular tachycardia
- Familial visceral myopathy
- Familial wilms tumor 2
Fan-Faz
- Fan death
- Fanconi anemia type 1
- Fanconi anemia type 2
- Fanconi anemia type 3
- Fanconi Bickel syndrome
- Fanconi ichthyosis dysmorphism
- Fanconi like syndrome
- Fanconi pancytopenia
- Fanconi syndrome
- Fanconi syndrome, renal, with nephrocalcinosis and renal stones
- Fanconi's anemia
- Fara Chlupackova syndrome
- Farber's disease
- Farmer's lung
- Fas deficiency
- Fascioliasis
- Fatal familial insomnia
- Fatty liver
- Faulk Epstein Jones syndrome
- Faye Petersen Ward Carey syndrome
- Fazio Londe syndrome
Fe
Fea-Fer
- Fealty syndrome
- Febrile seizure
- Fechtner syndrome
- Feigenbaum Bergeron Richardson syndrome
- Feigenbaum Bergeron syndrome
- Feingold syndrome
- Felty's Syndrome
- Female pseudohermaphrodism Genuardi type
- Female pseudohermaphroditism
- Femoral facial syndrome
- Femur bifid with monodactylous ectrodactyly
- Femur fibula ulna syndrome
- Fenton Wilkinson Toselano syndrome
- Ferlini Ragno Calzolari syndrome
- Fernhoff Blackston Oakley syndrome
- Ferrocalcinosis cerebro vascular
Fet
- Fetal acitretin syndrome
- Fetal akinesia syndrome X linked
- Fetal aminopterin syndrome
- Fetal and neonatal alloimmune thrombocytopenia
- Fetal antihypertensive drugs syndrome
- Fetal brain disruption sequence
- Fetal cytomegalovirus syndrome
- Fetal diethylstilbestrol syndrome
- Fetal edema
- Fetal enterovirus syndrome
- Fetal hydantoin syndrome
- Fetal indomethacin syndrome
- Fetal iodine syndrome
- Fetal left ventricular aneurysm
- Fetal methimazole syndrome
- Fetal methyl mercury syndrome
- Fetal minoxidil syndrome
- Fetal parainfluenza virus type 3 syndrome
- Fetal parvovirus syndrome
- Fetal phenothiazine syndrome
- Fetal prostaglandin syndrome
- Fetal thalidomide syndrome
- Fetal warfarin syndrome
Fg
Fi
Fib-Fil
- Fiber type disproportion, congenital
- Fibrinogen deficiency, congenital
- Fibrochondrogenesis
- Fibrolipomatosis
- Fibroma
- Fibromatosis gingival hypertrichosis
- Fibromatosis multiple non ossifying
- Fibromatosis
- Fibromuscular dysplasia of arteries
- Fibromuscular dysplasia
- Fibromyalgia
- Fibrosarcoma
- Fibrosing alveolitis
- Fibrosing Mediastinitis
- Fibrosis
- Fibrous dysplasia of bone
- Fibrous dysplasia
- Fibrodysplasia ossificans progressiva
- Fibula aplasia complex brachydactyly
- Fibular aplasia ectrodactyly
- Fibular hypoplasia femoral bowing oligodactyly
- Fibular hypoplasia scapulo pelvic dysplasia absent
- Filariasis
- Filippi syndrome
Fin-Fit
- Fine Lubinsky syndrome
- Fingerprints absence syndactyly milia
- Finnish lethal neonatal metabolic syndrome
- Finnish type amyloidosis
- Finucane Kurtz Scott syndrome
- Fish poisoning
- Fish-eye disease
- Fissured tongue
- Fistulous vegetative verrucous hydradenoma
- Fitz-Hugh-Curtis syndrome
- Fitzsimmons Walson Mellor syndrome
- Fitzsimmons-Guilbert syndrome
- Fitzsimmons-McLachlan-Gilbert syndrome
Fl
- Flavimonas oryzihabitans
- Flesh eating bacteria
- Floating limb syndrome
- Floating-harbor syndrome
- Florid cystic endosalpingiosis of the uterus
- Flotch syndrome
- Fluorosis
- Flynn Aird syndrome
Fo
- Focal agyria pachygyria
- Focal alopecia congenital megalencephaly
- Focal dermal hypoplasia
- Focal dystonia
- Focal facial dermal dysplasia
- Focal or multifocal malformations in neuronal migration
- Foix-Chavany-Marie syndrome
- Foix-Alajouanine syndrome
- Follicular atrophoderma-basal cell carcinoma
- Follicular Dendritic Cell Tumor
- Follicular hamartoma alopecia cystic fibrosis
- Follicular ichthyosis
- Follicular lymphoma
- Follicular lymphoreticuloma
- Fontaine Farriaux Blanckaert syndrome
- Forbes Albright syndrome
- Forbes disease
- Forestier's disease
- Formaldehyde poisoning
- Forney Robinson Pascoe syndrome
- Fountain syndrome
- Fowler Christmas Chapele syndrome
- Fox-Fordyce disease
Fr
Fra
- Fragile X syndrome type 1
- Fragile X syndrome type 2
- Fragile X syndrome type 3
- Fragile X syndrome
- Fragoso Cid Garcia Hernandez syndrome
- Franceschetti-Klein syndrome
- Francheschini Vardeu Guala syndrome
- Francois dyscephalic syndrome
- Franek Bocker kahlen syndrome
- Fraser Jequier Chen syndrome
- Fraser like syndrome
- Fraser syndrome
- Frasier syndrome
- FRAXA syndrome
- FRAXD
- FRAXE syndrome
Fre-Fri
- Free sialic acid storage disease
- Freeman-Sheldon syndrome
- Freiberg's disease
- Freire Maia odontotrichomelic syndrome
- Freire Maia Pinheiro Opitz syndrome
- Frenkel Russe syndrome
- Frey's syndrome
- Frias syndrome
- Fried Goldberg Mundel syndrome
- Friedel Heid Grosshans syndrome
- Friedman Goodman syndrome
- Friedreich ataxia congenital glaucoma
- Friedreich's ataxia
Fro-Fru
- Froelich's syndrome
- Frölich's syndrome
- Fronto nasal malformation cloacal exstrophy
- Frontofacionasal dysplasia type Al gazali
- Fronto-facio-nasal dysplasia
- Frontometaphyseal dysplasia
- Frontonasal dysplasia acromelic
- Frontonasal dysplasia klippel feil syndrome
- Frontonasal dysplasia phocomelic upper limbs
- Frontonasal dysplasia
- Frontotemporal dementia
- Froster huch syndrome
- Froster Iskenius Waterson syndrome
- Fructose intolerance
- Fructose-1,6-bisphosphatase deficiency
- Fructose-1-phosphate aldolase deficiency, heredita
- Fructosemia, hereditary
- Fructosuria
Fry
- Frydman Cohen Ashenazi syndrome
- Frydman Cohen Karmon syndrome
- Fryer syndrome
- Fryns Fabry Remans syndrome
- Fryns Hofkens Fabry syndrome
- Fryns smeets thiry syndrome
Fu
- Fucosidosis type 1
- Fucosidosis
- Fuhrmann Rieger De sousa syndrome
- Fukuda Miyanomae Nakata syndrome
- Fukuyama type muscular dystrophy
- Fumarase deficiency
- Fumaric aciduria
- Functioning pancreatic endocrine tumor
- Fuqua Berkovitz syndrome
- Furlong Kurczynski Hennessy syndrome
- Furukawa Takagi Nakao syndrome
- Furunculous myiasis
- Fused mandibular incisors