F

• Fabry disease

• FACES syndrome

• Facial asymmetry temporal seizures

• Facial clefting corpus callosum agenesis

• Facial ectodermal dysplasia

• Facial onset sensory and motor neuronopathy

• Facio digito genital syndrome recessive form

• Facio skeletal genital syndrome Rippberger type

• Facio thoraco genital syndrome

• Faciocardiomelic dysplasia lethal

• Faciocardiorenal syndrome

• Faciomandibular myoclonus, nocturnal

• Facioscapulohumeral muscular dystrophy

• Factor 2 deficiency

• Factor V deficiency

• Factor VII deficiency

• Factor X deficiency

• Factor XI deficiency

• Factor XII deficiency

• Factor XIII deficiency

• Fallopian tube cancer

• Fallot complex with severe mental and growth retardation

• Familial adenomatous polyposis

• Familial Alzheimer disease

• Familial amyloidosis, Finnish type

• Familial arteriosclerotic leukoencephalopathy, alopecia, lumbago without arterial hypertension

• Familial atrial fibrillation

• Familial avascular necrosis of the femoral head

• Familial band heterotopia

• Familial bilateral striatal necrosis

• Familial capillaro-venous leptomeningeal angiomatosis

• Familial caudal dysgenesis

• Familial cold autoinflammatory syndrome

• Familial colorectal cancer

• Familial congenital palsy of trochlear nerve

• Familial cutaneous collagenoma

• Familial cylindromatosis

• Familial deafness

• Familial dermographism

• Familial dilated cardiomyopathy

• Familial dysautonomia

• Familial encephalopathy with neuroserpin inclusion bodies

• Familial eosinophilia

• Familial episodic pain syndrome

• Familial erythema nodosum

• Familial exudative vitreoretinopathy

• Familial focal epilepsy with variable foci

• Familial glucocorticoid deficiency

• Familial HDL deficiency

• Familial hemiplegic migraine

• Familial hemiplegic migraine type 1

• Familial hemiplegic migraine type 2

• Familial hemiplegic migraine type 3

• Familial hyperaldosteronism type 2

• Familial hyperaldosteronism type III

• Familial hypersecretion of adrenal androgens

• Familial hyperthyroidism due to mutations in TSH receptor

• Familial hypertrophic cardiomyopathy

• Familial hypobetalipoproteinemia

• Familial hypocalciuric hypercalcemia

• Familial hypocalciuric hypercalcemia type 1

• Familial hypocalciuric hypercalcemia type 2

• Familial hypocalciuric hypercalcemia type 3

• Familial hypopituitarism

• Familial interstitial fibrosis

• Familial isolated hyperparathyroidism

• Familial isolated pituitary adenoma

• Familial joint instability syndrome

• Familial juvenile hyperuricaemic nephropathy

• Familial LCAT deficiency

• Familial lipoprotein lipase deficiency

• Familial Mediterranean fever

• Familial mixed cryoglobulinemia

• Familial multiple lipomatosis

• Familial multiple trichodiscomas

• Familial myelofibrosis

• Familial nasal acilia

• Familial neurocardiogenic syncope

• Familial osteochondritis dissecans

• Familial pancreatic cancer

• Familial partial lipodystrophy

• Familial partial lipodystrophy associated with PPARG mutations

• Familial partial lipodystrophy type 2

• Familial partial lipodystrophy type Köbberling

• Familial partial paralysis

• Familial pemphigus vulgaris

• Familial periodic paralysis

• Familial platelet disorder with associated myeloid malignancy

• Familial porencephaly

• Familial primary hypomagnesemia

• Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis

• Familial progressive cardiac conduction defect

• Familial prostate cancer

• Familial pulmonary arterial hypertension leucopenia and atrial septal defect

• Familial reactive perforating collagenosis

• Familial stomach cancer

• Familial streblodactyly

• Familial thoracic aortic aneurysm and dissection

• Familial thyroglossal duct cyst

• Familial transthyretin amyloidosis

• Familial tumoral calcinosis

• Familial ventricular tachycardia

• Familial visceral myopathy with external ophthalmoplegia

• Familial Wilms tumor 2

• Fanconi anemia

• Fanconi Bickel syndrome

• Fanconi syndrome

• Fara Chlupackova syndrome

• Farber's disease

• Farmer's lung

• Fascioliasis

• Fatal familial insomnia

• Fatal infantile encephalomyopathy

• Fatty acid hydroxylase-associated neurodegeneration

• Faulk Epstein Jones syndrome

• Faye-Petersen-Ward-Carey syndrome

• FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome

• Febrile infection-related epilepsy syndrome

• Febrile Ulceronecrotic Mucha-Habermann disease

• Feigenbaum Bergeron Richardson syndrome

• Feigenbaum Bergeron syndrome

• Feingold syndrome

• Feingold Trainer syndrome

• Felty's syndrome

• Femoral facial syndrome

• Femur bifid with monodactylous ectrodactyly

• Femur fibula ulna syndrome

• Fenton Wilkinson Toselano syndrome

• Fertile eunuch syndrome

• Fetal akinesia deformation sequence

• Fetal akinesia syndrome X-linked

• Fetal aminopterin syndrome

• Fetal and neonatal alloimmune thrombocytopenia

• Fetal brain disruption sequence

• Fetal cystic hygroma

• Fetal edema

• Fetal enterovirus syndrome

• Fetal hydantoin syndrome

• Fetal indomethacin syndrome

• Fetal iodine syndrome

• Fetal left ventricular aneurysm

• Fetal macrosomia

• Fetal methylmercury syndrome

• Fetal minoxidil syndrome

• Fetal parainfluenza virus type 3 syndrome

• Fetal parvovirus syndrome

• Fetal phenothiazine syndrome

• Fetal retinoid syndrome

• Fetal thalidomide syndrome

• Fetal valproate syndrome

• FG syndrome

• FG syndrome 2

• FG syndrome 3

• Fibrillary glomerulonephritis

• Fibrinogen deficiency, congenital

• Fibro-adipose vascular anomaly

• Fibrocartilaginous embolism

• Fibrochondrogenesis

• Fibrodysplasia ossificans progressiva

• Fibrolamellar carcinoma

• Fibromatosis multiple non ossifying

• Fibrosarcoma

• Fibrosing mediastinitis

• Fibrous dysplasia

• Fibula aplasia complex brachydactyly

• Fibular aplasia

• Fibular aplasia ectrodactyly

• Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome

• Fibular hypoplasia and complex brachydactyly

• Fibular hypoplasia scapulo pelvic dysplasia absent

• Filippi syndrome

• Fine-Lubinsky syndrome

• Fingerprint body myopathy

• Fish-eye disease

• Fitz-Hugh-Curtis syndrome

• Fitzsimmons syndrome

• Fitzsimmons Walson Mellor syndrome

• Fitzsimmons-Guilbert syndrome

• Flat umbilicus familial

• Flavimonas oryzihabitans infection

• Floating-Harbor syndrome

• Florid cemento-osseous dysplasia

• Florid cystic endosalpingiosis of the uterus

• Florid papillomatosis of the nipple

• FLOTCH syndrome

• Flynn Aird syndrome

• FMR1-related primary ovarian insufficiency

• Focal alopecia congenital megalencephaly

• Focal cortical dysplasia of Taylor

• Focal dermal hypoplasia

• Focal facial dermal dysplasia

• Focal or multifocal malformations in neuronal migration

• Focal palmoplantar and gingival keratoderma

• Focal segmental glomerulosclerosis

• Foix Chavany Marie syndrome

• Follicle-stimulating hormone deficiency, isolated

• Follicular lymphoma

• Follicular lymphoreticuloma

• Fontaine Farriaux Blanckaert syndrome

• Formaldehyde poisoning

• Fountain syndrome

• Fournier gangrene

• Fowler's syndrome

• Fox-Fordyce disease

• FOXG1 syndrome

• Fragile X syndrome

• Fragile X syndrome type 1

• Fragile X syndrome type 2

• Fragile X syndrome type 3

• Fragile XE syndrome

• Franceschini Vardeu Guala syndrome

• Frank Ter Haar syndrome

• Fraser Jequier Chen syndrome

• Fraser syndrome

• Frasier syndrome

• FRAXD

• Free sialic acid storage disease

• Freeman Sheldon syndrome

• Freiberg's disease

• Frenkel Russe syndrome

• Frey's syndrome

• Frias syndrome

• Friedel Heid Grosshans syndrome

• Friedman Goodman syndrome

• Friedreich ataxia

• Frints De Smet Fabry Fryns syndrome

• Froelich syndrome

• Frontal fibrosing alopecia

• Fronto nasal malformation cloacal exstrophy

• Frontofacionasal dysplasia

• Frontometaphyseal dysplasia

• Frontonasal dysplasia

• Frontonasal dysplasia acromelic

• Frontonasal dysplasia Klippel Feil syndrome

• Frontonasal dysplasia phocomelic upper limbs

• Frontotemporal dementia

• Frontotemporal dementia, ubiquitin-positive

• Froster-Huch syndrome

• Fructose-1,6-bisphosphatase deficiency

• Fryns Fabry Remans syndrome

• Fryns Hofkens Fabry syndrome

• Fryns smeets thiry syndrome

• Fryns syndrome

• Fuchs heterochromic iridocyclitis

• Fucosidosis

• Fucosidosis type 1

• Fuhrmann syndrome

• Fukuda Miyanomae Nakata syndrome

• Fukuyama type muscular dystrophy

• Fumarase deficiency

• Functioning pancreatic endocrine tumor

• Fundus dystrophy, pseudoinflammatory, of Sorsby

• Fuqua Berkovitz syndrome

• Furunculous myiasis

• Fused mandibular incisors