FANDOM


Fabry disease [↗]
Faces syndrome [↗]
Facial asymmetry - temporal seizures [↗]
Facial dermoid cyst [↗]
Facial dysmorphism - ambiguous genitalia - hypopituitarism - short limbs [↗]
Facial dysmorphism - intellectual deficit - short stature - hearing loss [↗]
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation [↗]
Facial dysmorphism - shawl scrotum - joint laxity [↗]
Facial ectodermal dysplasia [↗]
Facial hemispasm [↗]
Facial onset sensory and motor neuronopathy [↗]
Facio-audio-symphalangism [↗]
Facioauriculovertebral dysplasia [↗]
Faciocardiorenal syndrome [↗]
Faciocutaneoskeletal syndrome [↗]
Faciodigitogenital syndrome [↗]
Facio-digito-genital syndrome, Kuwait type [↗]
Faciogenital dysplasia [↗]
Facio-genito-popliteal syndrome [↗]
Facio-oculo-acoustico-renal syndrome [↗]
Facio-oculo-acoustico-renal syndrome [↗]
Facio-pharyngo-glosso-masticatory diplegia [↗]
Facioscapulohumeral dystrophy [↗]
Facioscapulohumeral muscular dystrophy [↗]
Facioscapulohumeral myopathy [↗]
Facio-skeletal-genital syndrome, Rippberger type [↗]
Facio-thoraco-genital syndrome [↗]
Factor IX deficiency [↗]
Factor VIII deficiency [↗]
Factor V Quebec [↗]
FADS [↗]
Failure of teeth eruption [↗]
Faisalabad histiocytosis [↗]
Fallot complex - intellectual deficit - growth delay [↗]
Familial abdominal aortic aneurysm [↗]
Familial acoustic neurinoma [↗]
Familial acoustic neuroma [↗]
Familial acute necrotizing encephalopathy [↗]
Familial adenomatous polyposis [↗]
Familial adenomatous polyposis due to 5q22.2 microdeletion [↗]
Familial adenomatous polyposis due to del(5)(q22.2) [↗]
Familial adenomatous polyposis due to monosomy 5q22.2 [↗]
Familial adrenal adenoma [↗]
Familial adrenal hypoplasia [↗]
Familial adrenal hypoplasia, miniature type [↗]
Familial advanced sleep-phase syndrome [↗]
Familial afibrinogenemia [↗]
Familial Alzheimer disease [↗]
Familial amyloid nephropathy [↗]
Familial amyloid nephropathy due to Apolipoprotein AII variant [↗]
Familial amyloid nephropathy due to Apolipoprotein AI variant [↗]
Familial amyloid nephropathy due to fibrinogen A alpha-chain variant [↗]
Familial amyloid nephropathy due to lysozyme variant [↗]
Familial amyloidosis, Finnish type [↗]
Familial amyloid polyneuropathy [↗]
Familial amyloid polyneuropathy type 4 [↗]
Familial anetoderma [↗]
Familial angiolipomatosis [↗]
Familial angioma serpiginosum [↗]
Familial angioneurotic edema [↗]
Familial aortic dissection [↗]
Familial articular chondrocalcinosis [↗]
Familial articular chondrocalcinosis type 1 [↗]
Familial articular chondrocalcinosis type 2 [↗]
Familial atrial fibrillation [↗]
Familial atrial myxoma [↗]
Familial avascular necrosis of femoral head [↗]
Familial benign cervical lipomatosis [↗]
Familial benign chronic pemphigus [↗]
Familial benign Copper deficiency [↗]
Familial benign hypercalcemia [↗]
Familial berry aneurysm [↗]
Familial brain cavernous angioma [↗]
Familial breast cancer [↗]
Familial breast carcinoma [↗]
Familial capillary hemangioma [↗]
Familial caudal dysgenesis [↗]
Familial CD8 deficiency [↗]
Familial cerebello-retinal angiomatosis [↗]
Familial cerebral cavernoma [↗]
Familial cerebral cavernous malformation [↗]
Familial cerebral saccular aneurysm [↗]
Familial cerebral vascular accident [↗]
Familial chondromalacia patellae [↗]
Familial cold autoinflammatory syndrome [↗]
Familial cold autoinflammatory syndrome 2 [↗]
Familial cold urticaria [↗]
Familial congenital controlateral synkinesia [↗]
Familial congenital hypopituitarism [↗]
Familial congenital mirror movements [↗]
Familial congenital palsy of trochlear nerve [↗]
Familial cutaneous collagenoma [↗]
Familial cylindromatosis [↗]
Familial dementia, British type [↗]
Familial dementia, Danish type [↗]
Familial developmental dysphasia [↗]
Familial digital arthropathy-brachydactyly [↗]
Familial distal primary acidosis [↗]
Familial doughnut lesions of skull [↗]
Familial drusen [↗]
Familial Dupuytren contracture [↗]
Familial dysautonomia [↗]
Familial dysfibrinogenemia [↗]
Familial ectopic ossification [↗]
Familial encephalopathy with neuroserpin inclusion bodies [↗]
Familial erythrocytosis [↗]
Familial esophageal achalasia [↗]
Familial essential thrombocythemia [↗]
Familial expansile osteolysis [↗]
Familial exudative vitreoretinopathy [↗]
Familial gastric cancer [↗]
Familial generalized lentiginosis [↗]
Familial gestational hyperthyroidism [↗]
Familial glucocorticoid deficiency [↗]
Familial gonadotropin-independent male-limited sexual precocity [↗]
Familial hemophagocytic lymphohistiocytosis [↗]
Familial hibernian fever [↗]
Familial hyperaldosteronism type 1 [↗]
Familial hyperaldosteronism type 2 [↗]
Familial hyperaldosteronism type 3 [↗]
Familial hyperalphalipoproteinemia [↗]
Familial hypercalcemia - nephrocalcinosis - indicanuria [↗]
Familial hypercholanemia [↗]
Familial hyperchylomicronemia [↗]
Familial hyperestrogenism [↗]
Familial hyperkalemic hypertension [↗]
Familial hyperkalemic periodic paralysis [↗]
Familial HyperPP [↗]
Familial hyperreninemic hypoaldosteronism type 1 [↗]
Familial hyperreninemic hypoaldosteronism type 2 [↗]
Familial hyperthyroidism due to mutations in TSH receptor [↗]
Familial hypertriglyceridemia [↗]
Familial hypoaldosteronism [↗]
Familial hypoalphalipoproteinemia [↗]
Familial hypocalciuric hypercalcemia [↗]
Familial hypocalciuric hypercalcemia type 1 [↗]
Familial hypocalciuric hypercalcemia type 2 [↗]
Familial hypocalciuric hypercalcemia type 3 [↗]
Familial hypodysfibrinogenemia [↗]
Familial hypofibrinogenemia [↗]
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement [↗]
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis [↗]
Familial hypospadias [↗]
Familial IBSN [↗]
Familial idiopathic dilatation of the right atrium [↗]
Familial idiopathic nephrotic syndrome [↗]
Familial idiopathic steroid-resistant nephrotic syndrome [↗]
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation [↗]
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis [↗]
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis [↗]
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis [↗]
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes [↗]
Familial infantile bilateral striatal necrosis [↗]
Familial infantile striatonigral necrosis [↗]
Familial intestinal malrotation - facial anomalies [↗]
Familial intestinal polyatresia syndrome [↗]
Familial isolated arrhythmogenic right ventricular cardiomyopathy [↗]
Familial isolated arrhythmogenic right ventricular dysplasia [↗]
Familial isolated ARVC [↗]
Familial isolated ARVD [↗]
Familial isolated clubfoot due to 17q23.1q23.2 microduplication [↗]
Familial isolated congenital asplenia [↗]
Familial isolated dilated cardiomyopathy [↗]
Familial isolated hyperparathyroidism [↗]
Familial isolated hypoparathyroidism [↗]
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland [↗]
Familial isolated hypoparathyroidism due to impaired PTH secretion [↗]
Familial isolated restrictive cardiomyopathy [↗]
Familial isolated vitamin E deficiency [↗]
Familial joint instability syndrome [↗]
Familial joint laxity [↗]
Familial juvenile gigantomastia [↗]
Familial juvenile gouty nephropathy [↗]
Familial juvenile hypertrophy of the breast [↗]
Familial juvenile hyperuricemic nephropathy type 1 [↗]
Familial juvenile hyperuricemic nephropathy type 2 [↗]
Familial keratoacanthoma [↗]
Familial lambdoid synostosis [↗]
Familial LCAT deficiency [↗]
Familial leiomyomatosis [↗]
Familial leiomyomatosis with renal carcinoma [↗]
Familial leiomyomatosis with renal cell cancer [↗]
Familial lentigines profusa [↗]
Familial long QT syndrome [↗]
Familial lupus anticoagulant [↗]
Familial macular edema [↗]
Familial mediterranean fever [↗]
Familial medullary thyroid carcinoma [↗]
Familial megaloblastic anemia [↗]
Familial melanoma [↗]
Familial mesial temporal lobe epilepsy with febrile seizures [↗]
Familial mitral valve prolapse [↗]
Familial MTC [↗]
Familial multinodular goiter [↗]
Familial multiple coagulation factor deficiency [↗]
Familial multiple cutaneous leiomyomas [↗]
Familial multiple fibrofolliculoma [↗]
Familial multiple lentigines syndrome [↗]
Familial multiple lentigines syndrome without systemic involvement [↗]
Familial multiple lipomatosis [↗]
Familial multiple meningioma [↗]
Familial multiple trichoepithelioma [↗]
Familial nasal acilia [↗]
Familial nephropathy with gout [↗]
Familial non-immune hyperthyroidism [↗]
Familial nonpolyposis colon cancer [↗]
Familial nonpolyposis colorectal cancer [↗]
Familial ocular anterior segment mesenchymal dysgenesis [↗]
Familial omphalocele syndrome with facial dysmorphism [↗]
Familial or idiopathic dilated cardiomyopathy [↗]
Familial or idiopathic restrictive cardiomyopathy [↗]
Familial or sporadic hemiplegic migraine [↗]
Familial osteochondritis dissecans [↗]
Familial osteodysplasia, Anderson type [↗]
Familial osteoectasia [↗]
Familial osteonecrosis of the femoral head [↗]
Familial otodentodysplasia [↗]
Familial pancreatic cancer [↗]
Familial pancreatic carcinoma [↗]
Familial papillary renal cell carcinoma [↗]
Familial parathyroid adenoma [↗]
Familial parathyroids hyperplasia [↗]
Familial Parkinson disease [↗]
Familial Parkinson's disease dementia [↗]
Familial paroxysmal ataxia [↗]
Familial paroxysmal ventricular fibrillation, not Brugada type [↗]
Familial partial epilepsy [↗]
Familial partial epilepsy with variable focus [↗]
Familial partial lipodystrophy associated with PLIN1 mutations [↗]
Familial partial lipodystrophy associated with PPARG mutations [↗]
Familial partial lipodystrophy due to AKT2 mutations [↗]
Familial partial lipodystrophy, Dunnigan type [↗]
Familial partial lipodystrophy, Köbberling type [↗]
Familial partial lipodystrophy type 1 [↗]
Familial partial lipodystrophy type 2 [↗]
Familial partial lipodystrophy type 3 [↗]
Familial patella aplasia-hypoplasia [↗]
Familial pelvis-scapular dysplasia [↗]
Familial pheochromocytoma-paraganglioma [↗]
Familial platelet disorder with associated myeloid malignancy [↗]
Familial platelet syndrome [↗]
Familial platelet syndrome with predisposition to acute myelogenous leukemia [↗]
Familial polyposis coli [↗]
Familial polyposis coli due to monosomy 5q22.2 [↗]
Familial porencephaly [↗]
Familial primary hyperparathyroidism [↗]
Familial primary hypomagnesemia [↗]
Familial primary pulmonary hypoplasia [↗]
Familial prion disease Alzheimer-like [↗]
Familial progressive cardiac conduction defect [↗]
Familial progressive heart block [↗]
Familial progressive hyper- and hypopigmentation [↗]
Familial progressive hyperpigmentation [↗]
Familial progressive vestibulocochlear dysfunction [↗]
Familial prolactinoma [↗]
Familial prostate cancer [↗]
Familial pseudohyperkalemia [↗]
Familial pseudohyperkalemia, Cardiff type [↗]
Familial pseudohyperkalemia type 1 [↗]
Familial pseudohyperkalemia type 2 [↗]
Familial pulmonary arterial hypertension [↗]
Familial pure proximal renal tubular acidosis [↗]
Familial pyrimidinemia [↗]
Familial reactive perforating collagenosis [↗]
Familial rectal pain [↗]
Familial recurrent arthritis [↗]
Familial recurrent peripheral facial palsy [↗]
Familial renal amyloidosis [↗]
Familial renal amyloidosis due to Apolipoprotein AII variant [↗]
Familial renal amyloidosis due to Apolipoprotein AI variant [↗]
Familial renal amyloidosis due to fibrinogen A alpha-chain variant [↗]
Familial renal amyloidosis due to lysozyme variant [↗]
Familial renal cell carcinoma [↗]
Familial renal glucosuria [↗]
Familial restrictive cardiomyopathy type 1 [↗]
Familial restrictive cardiomyopathy type 2 [↗]
Familial restrictive cardiomyopathy type 3 [↗]
Familial rhabdoid tumor [↗]
Familial Rosaï-Dorfman disease [↗]
Familial scaphocephaly - radioulnar synostosis [↗]
Familial scaphocephaly syndrome, McGillivray type [↗]
Familial Scheuermann disease [↗]
Familial Scheuermann juvenile kyphosis [↗]
Familial segmental neurofibromatosis [↗]
Familial SHML [↗]
Familial short QT syndrome [↗]
Familial sinus histiocytosis with massive lymphadenopathy [↗]
Familial spastic paraplegia [↗]
Familial spinal neurofibromatosis [↗]
Familial spinal osteochondrosis [↗]
Familial spontaneous pneumothorax [↗]
Familial Startle disease [↗]
Familial steroid-resistant nephrotic syndrome with sensorineural deafness [↗]
Familial stomach cancer [↗]
Familial supernumerary nipples [↗]
Familial symmetric lipomatosis [↗]
Familial temporal epilepsy [↗]
Familial thoracic aortic aneurysm [↗]
Familial thoracic aortic aneurysm and/or dissection [↗]
Familial thrombocythemia [↗]
Familial thrombocytosis [↗]
Familial thrombomodulin anomalies [↗]
Familial thyroglossal duct cyst [↗]
Familial thyroid dyshormonogenesis [↗]
Familial trembling of the chin [↗]
Familial triphalangeal thumbs - duplication of the big toes [↗]
Familial vascular leukoencephalopathy [↗]
Familial vestibular schwannoma [↗]
Familial visceral myopathy [↗]
Familial vocal cord dysfunction [↗]
Familial woolly hair syndrome [↗]
Familial wooly hair syndrome [↗]
Fanconi anemia [↗]
Fanconi-Bickel disease [↗]
Fanconi pancytopenia [↗]
Fanconi syndrome - ichthyosis - dysmorphism [↗]
Fantasy Island syndrome [↗]
FAP [↗]
FAP due to monosomy 5q22.2 [↗]
Fara-Chlupackova syndrome [↗]
Farber lipogranulomatosis [↗]
Farmer's lung disease [↗]
FAS deficiency [↗]
FASPS [↗]
FASTKD2-related infantile mitochondrial encephalomyopathy [↗]
Fatal familial insomnia [↗]
Fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency [↗]
Fatal infantile COX deficiency [↗]
Fatal infantile cytochrome C oxidase deficiency [↗]
Fatal infantile encephalopathy, with mitochondrial respiratory chain defects [↗]
Fatal infantile encephalopathy with olivopontocerebellar hypoplasia [↗]
Fatal infantile hypertonic myofibrillar myopathy [↗]
Fatal infantile lactic acidosis with methylmalonic aciduria [↗]
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 [↗]
Fatty acid alcohol oxidoreductase deficiency [↗]
Faulk-Epstein-Jones syndrome [↗]
Fazio-Londe disease [↗]
FCAS [↗]
FCAS2 [↗]
FCD type I [↗]
FCD type Ia [↗]
FCD type Ib [↗]
FCD type Ic [↗]
FCD type II [↗]
FCD type IIa [↗]
FCD type IIb [↗]
FCMD [↗]
FCS syndrome [↗]
FCU [↗]
Fechtner syndrome [↗]
FED [↗]
Feer disease [↗]
Feigenbaum-Bergeron-Richardson syndrome [↗]
Feingold syndrome [↗]
Felty syndrome [↗]
Female pseudohermaphrodism - anorectal anomalies [↗]
Female pseudohermaphroditism - skeletal anomalies [↗]
Female restricted epilepsy with intellectual deficit [↗]
Femoral-facial syndrome [↗]
Femoral hypoplasia - unusual facies syndrome [↗]
Femur-fibula-ulna complex [↗]
Femur-fibula-ulna dysostosis [↗]
Femur-fibula-ulna syndrome [↗]
FENIB [↗]
Fenton-Wilkinson-Toselano syndrome [↗]
FEOM [↗]
Ferlini-Ragno-Calzolari syndrome [↗]
Fernhoff-Blackston-Oakley syndrome [↗]
Ferritin-related neurodegeneration [↗]
Ferrocalcinosis cerebro vascular [↗]
Ferroportin disease [↗]
Fetal acitretin syndrome [↗]
Fetal akinesia deformation sequence [↗]
Fetal alcohol syndrome [↗]
Fetal aminopterin syndrome [↗]
Fetal and neonatal alloimmune thrombocytopenia [↗]
Fetal brain disruption sequence [↗]
Fetal cocaine syndrome [↗]
Fetal cytomegalovirus syndrome [↗]
Fetal dihydantoin syndrome [↗]
Fetal edema [↗]
Fetal face syndrome [↗]
Fetal Gaucher disease [↗]
Fetal hydantoin syndrome [↗]
Fetal indomethacin syndrome [↗]
Fetal iodine syndrome [↗]
Fetal left ventricular aneurysm [↗]
Fetal methylmercury syndrome [↗]
Fetal minoxidil syndrome [↗]
Fetal-onset olivopontocerebellar hypoplasia [↗]
Fetal ovarian cyst [↗]
Fetal parvovirus syndrome [↗]
Fetal thalidomide syndrome [↗]
Fetal trimethadione syndrome [↗]
Fetal valproate syndrome [↗]
Fetal valproic acid syndrome [↗]
Fetal varicella syndrome [↗]
Fetal warfarin syndrome [↗]
Feto-fetal transfusion syndrome [↗]
Fever-induced resistant epilepsy in school-age children [↗]
FEVR [↗]
FFA [↗]
FFDD type I [↗]
FFS [↗]
FFU complex [↗]
FG syndrome type 1 [↗]
FH1 [↗]
FH2 [↗]
FHC [↗]
FHC [↗]
FHHA1 [↗]
FHHA2 [↗]
FHI [↗]
FHUFS [↗]
Fibrillary astrocytoma [↗]
Fibrinogen A alpha-chain amyloidosis [↗]
Fibrin-stabilizing factor deficiency [↗]
Fibrocalculous pancreatopathy [↗]
Fibrochondrogenesis [↗]
Fibrodysplasia ossificans progressiva [↗]
Fibrofolliculomas with trichodiscomas and acrochordons [↗]
Fibromuscular dysplasia of arteries [↗]
Fibromyxosarcoma [↗]
Fibronectin glomerulopathy [↗]
Fibrosarcoma [↗]
Fibrosing mediastinitis [↗]
Fibrous dysplasia of bone [↗]
Fibular aplasia - complex brachydactyly [↗]
Fibular aplasia - ectrodactyly [↗]
Fibular dimelia - diplopodia [↗]
Fibular hemimelia [↗]
Fibular hypoplasia or aplasia - femoral bowing - oligodactyly [↗]
Fibulo-ulnar hypoplasia - renal anomalies [↗]
FIC1 deficiency [↗]
Fiessinger-Leroy disease [↗]
Fiessinger-Leroy-Reiter's syndrome [↗]
Figuera syndrome [↗]
FIHPT [↗]
Filariasis [↗]
Filippi syndrome [↗]
Fine-Lubinsky syndrome [↗]
Fingerprint body myopathy [↗]
Finkel disease [↗]
Finlay-Markes syndrome [↗]
Finnish congenital nephrosis [↗]
Finucane-Kurtz-Scott syndrome [↗]
FIRES [↗]
First branchial arch syndrome [↗]
First branchial cleft anomaly [↗]
First branchial cleft cyst [↗]
First branchial cleft fistula [↗]
Fisher syndrome [↗]
Fish-eye disease [↗]
Fish-odor syndrome [↗]
Fistulous vegetative verrucous hydradenoma [↗]
Fitzsimmons-Guilbert syndrome [↗]
Fitzsimmons-McLachlan-Gilbert syndrome [↗]
Fitzsimmons-Walson-Mellor syndrome [↗]
Fixed subaortic stenosis [↗]
FJHN type 1 [↗]
FJHN type 2 [↗]
Flat face - microstomia - ear anomaly [↗]
FLD [↗]
Flegel disease [↗]
Floating-Harbor syndrome [↗]
Florid cemento-osseous dysplasia [↗]
Florid osseous dysplasia [↗]
FLOTCH syndrome [↗]
Fluctuating myotonia [↗]
Flynn-Aird syndrome [↗]
FMF [↗]
Foamy myocardial transformation of infancy [↗]
FOAR syndrome [↗]
Focal alopecia congenital megalencephaly [↗]
Focal cemento-osseous dysplasia [↗]
Focal dermal hypoplasia [↗]
Focal dystonia [↗]
Focal facial dermal dysplasia [↗]
Focal facial dermal dysplasia type 2 [↗]
Focal myoclonus of face [↗]
Focal myositis [↗]
Foix-Alajouanine syndrome [↗]
Foix-Chavany-Marie syndrome [↗]
Folinic acid-responsive seizures [↗]
Follicular atrophoderma-basal cell carcinoma [↗]
Follicular dendritic cell sarcoma [↗]
Follicular dyskeratoma [↗]
Follicular hamartoma - alopecia - cystic fibrosis [↗]
Follicular ichthyosis [↗]
Follicular lichen planus [↗]
Follicular lymphoma [↗]
Follicular stimulating hormone-resistant ovaries [↗]
Folliculitis ulerythematosa reticulate [↗]
Folliculotropic mycosis fungoides [↗]
Foodborne botulism [↗]
FOP [↗]
Foramina parietalia permagna [↗]
Forbe disease [↗]
Foregut duplication cyst of the tongue [↗]
Formiminoglutamic aciduria [↗]
Formiminotransferase cyclodeaminase deficiency [↗]
Forney-Robinson-Pascoe syndrome [↗]
Forsius-Eriksson syndrome [↗]
FOSMN syndrome [↗]
Fountain syndrome [↗]
Fourth branchial cleft anomaly [↗]
Fourth branchial cleft cyst [↗]
Fourth branchial cleft fistula [↗]
Foveal hypoplasia - presenile cataract [↗]
Fowler-Christmas-Chapple syndrome [↗]
Fowler syndrome [↗]
FOXP2-associated dysphasia [↗]
FPAH [↗]
FPHH [↗]
FPLD1 [↗]
FPLD2 [↗]
FPLD3 [↗]
FPS/AML syndrome [↗]
FRA [↗]
Fragile X-associated tremor/ataxia syndrome [↗]
Fragile X syndrome [↗]
Fragoso-Cid-Garcia-Hernandez syndrome [↗]
Franceschetti-Klein syndrome [↗]
François dyscephalic syndrome [↗]
Francois syndrome [↗]
Franek-Bocker-Kahlen syndrome [↗]
Franklin disease [↗]
Frank-Ter Haar syndrome [↗]
Fraser-like syndrome [↗]
Fraser syndrome [↗]
Frasier syndrome [↗]
FRAXA syndrome [↗]
FRAXE intellectual deficiency [↗]
FRAXF syndrome [↗]
FraX syndrome [↗]
Freeman-Sheldon syndrome [↗]
Freeman-Sheldon syndrome variant [↗]
Free sialic acid storage disease [↗]
Freire Maia-Pinheiro-Opitz syndrome [↗]
Freire-Maia syndrome [↗]
Frias syndrome [↗]
Frieddman-Goodman syndrome [↗]
Fried-Goldberg-Mundel syndrome [↗]
Friedreich ataxia [↗]
Friedreich-like ataxia with selective vitamin E deficiency [↗]
Fried syndrome [↗]
Frontal encephalocele [↗]
Frontal fibrosing alopecia [↗]
Fronto-facio-nasal dysostosis [↗]
Frontofacionasal dysplasia [↗]
Frontometaphyseal dysplasia [↗]
Frontonasal arteriovenous malformation [↗]
Frontonasal dysplasia [↗]
Frontonasal dysplasia - Klippel-Feil syndrome [↗]
Frontonasal dysplasia with alopecia and genital abnomality [↗]
Frontonasal dysplasia with alopecia and genital anomaly [↗]
Frontotemporal dementia [↗]
Frontotemporal dementia and parkinsonism linked to chromosome 17 [↗]
Frontotemporal dementia with amyotrophic lateral sclerosis [↗]
Frontotemporal dementia with motor neuron disease [↗]
Frontotemporal dementia with motor neuron-disease type inclusions [↗]
Froster-Huch syndrome [↗]
Froster-Iskenius-Waterson syndrome [↗]
Fructokinase deficiency [↗]
Fructose-1,6-bisphosphatase deficiency [↗]
Fructose intolerance [↗]
Fructosuria [↗]
Frydman-Cohen-Karmon syndrome [↗]
Fryns-Aftimos syndrome [↗]
Fryns-Hofkens-Fabry syndrome [↗]
Fryns macrocephaly [↗]
Fryns microphthalmia syndrome [↗]
Fryns-Smeets-Thiry syndrome [↗]
Fryns syndrome [↗]
FSHD [↗]
FSH dystrophy [↗]
FSH-RO [↗]
F syndrome [↗]
FTCD deficiency [↗]
FTD [↗]
FTD-ALS [↗]
FTD-MND [↗]
FTDP-17 [↗]
FTH1-associated iron overload [↗]
FTH1-related iron overload [↗]
FTLD-MND [↗]
Fuchs endothelial corneal dystrophy [↗]
Fuchs heterochromic iridocyclitis [↗]
Fucosidosis [↗]
Fuhrmann-Rieger-de Sousa syndrome [↗]
Fuhrmann syndrome [↗]
Fukuda-Miyanomae-Nakata syndrome [↗]
Fukuhara syndrome [↗]
Fukuyama congenital muscular dystrophy [↗]
Fulminant viral hepatitis [↗]
Fumarase deficiency [↗]
Fumaric aciduria [↗]
Fumarylacetoacetase deficiency [↗]
Fundus albipunctatus [↗]
Fundus flavimaculatus [↗]
Fundus pulverulentus [↗]
Fuqua-Berkovitz syndrome [↗]
Furlong syndrome [↗]
Furukawa-Takagi-Nakao syndrome [↗]
Furuncular myiasis [↗]
Furunculoid myiasis [↗]
Furunculous myiasis [↗]
Fusariosis [↗]
Fusarium infection [↗]
Fused mandibular incisors [↗]
FV and FVIII combined deficiency [↗]
FXS [↗]
FXTAS syndrome [↗]

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