HealthSignal
Rare conditions starting with F
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289 conditions starting with F
- Fabry disease
- Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome
- Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
- Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome
- Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome
- Facial dysmorphism-shawl scrotum-joint laxity syndrome
- Facial hemiatrophy
- Facial onset sensory and motor neuronopathy
- Faciocardiorenal syndrome
- Faciodigitogenital syndrome
- Facioscapulohumeral muscular dystrophy
- Faciothoracogenital syndrome
- Factor I deficiency
- Factor V deficiency
- Factor VII deficiency
- Factor X deficiency
- Factor XI deficiency
- Factor XII deficiency disease
- Factor XIII deficiency
- FADD-related immunodeficiency
- Fallopian tube cancer
- Fallot complex-intellectual disability-growth delay syndrome
- Familial abdominal aortic aneurysm
- Familial acute necrotizing encephalopathy
- Familial adenomatous polyposis 2
- Familial adenomatous polyposis 3
- Familial adrenal hypoplasia with absent pituitary luteinizing hormone
- Familial Alzheimer-like prion disease
- Familial amyloid nephropathy with urticaria AND deafness
- Familial anetoderma
- Familial angiolipomatosis
- Familial apolipoprotein C-II deficiency
- Familial atrial fibrillation
- Familial atrial myxoma
- Familial atrioventricular septal defect
- Familial atypical multiple mole melanoma syndrome
- Familial avascular necrosis of the femoral head
- Familial benign copper deficiency
- Familial benign flecked retina
- Familial benign pemphigus
- Familial bicuspid aortic valve
- Familial cancer of breast
- Familial caudal dysgenesis
- Familial cavitary optic disk anomaly
- Familial cervical artery dissection
- Familial chilblain lupus
- Familial chronic myelocytic leukemia-like syndrome
- Familial chylomicronemia syndrome
- Familial clubfoot with or without associated lower limb anomalies
- Familial cold autoinflammatory syndrome
- Familial cold autoinflammatory syndrome 2
- Familial cold autoinflammatory syndrome 3
- Familial colorectal cancer
- Familial colorectal cancer type X
- Familial congenital nasolacrimal duct obstruction
- Familial congenital palsy of trochlear nerve
- Familial cutaneous collagenoma
- Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
- Familial developmental dysphasia
- Familial digital arthropathy-brachydactyly
- Familial dysautonomia
- Familial dysfibrinogenemia
- Familial encephalopathy with neuroserpin inclusion bodies
- Familial episodic pain syndrome
- Familial erythrocytosis
- Familial expansile osteolysis
- Familial exudative vitreoretinopathy
- Familial focal epilepsy with variable foci
- Familial generalized lentiginosis
- Familial gestational hyperthyroidism
- Familial glucocorticoid deficiency
- Familial hemiplegic migraine
- Familial hemolytic anemia
- Familial hemophagocytic lymphohistiocytosis
- Familial hemophagocytic lymphohistiocytosis type 1
- Familial hyperaldosteronism
- Familial hyperaldosteronism type II
- Familial hyperaldosteronism type III
- Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome
- Familial hyperprolactinemia
- Familial hyperthyroidism due to mutations in TSH receptor
- Familial hypertryptophanemia
- Familial hypoaldosteronism
- Familial hypobetalipoproteinemia 1
- Familial hypobetalipoproteinemia 2
- Familial hypocalciuric hypercalcemia
- Familial hypocalciuric hypercalcemia 1
- Familial hypocalciuric hypercalcemia 2
- Familial hypocalciuric hypercalcemia 3
- Familial hypofibrinogenemia
- Familial hypokalemia-hypomagnesemia
- Familial hypoparathyroidism
- Familial idiopathic dilatation of the right atrium
- Familial idiopathic steroid-resistant nephrotic syndrome
- Familial infantile bilateral striatal necrosis
- Familial infantile myoclonic epilepsy
- Familial isolated arrhythmogenic right ventricular dysplasia
- Familial isolated congenital asplenia
- Familial isolated deficiency of vitamin E
- Familial isolated hyperparathyroidism
- Familial isolated pituitary adenoma
- Familial isolated trichomegaly
- Familial juvenile hypertrophy of the breast
- Familial juvenile hyperuricemic nephropathy type 1
- Familial juvenile hyperuricemic nephropathy type 2
- Familial keratoacanthoma
- Familial median cleft of the upper and lower lips
- Familial melanoma
- Familial mitral valve prolapse
- Familial multiple discoid fibromas
- Familial multiple fibrofolliculoma
- Familial multiple lipomatosis
- Familial multiple nevi flammei
- Familial multiple polyposis syndrome
- Familial multiple trichoepitheliomata
- Familial nasal acilia
- Familial omphalocele syndrome with facial dysmorphism
- Familial or sporadic hemiplegic migraine
- Familial osteoarthropathy of the fingers
- Familial osteodysplasia, Anderson type
- Familial pancreatic carcinoma
- Familial papillary or follicular thyroid carcinoma
- Familial papillary thyroid carcinoma with renal papillary neoplasia
- Familial partial epilepsy
- Familial partial lipodystrophy
- Familial partial lipodystrophy, Dunnigan type
- Familial partial lipodystrophy, Kobberling type
- Familial pityriasis rubra pilaris
- Familial porencephaly
- Familial porphyria cutanea tarda
- Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- Familial primary localized cutaneous amyloidosis
- Familial progressive hyper- and hypopigmentation
- Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome
- Familial prostate carcinoma
- Familial pseudohyperkalemia
- Familial pterygium of the conjunctiva
- Familial reactive perforating collagenosis
- Familial recurrent peripheral facial palsy
- Familial renal glucosuria
- Familial renal hypouricemia
- Familial restrictive cardiomyopathy
- Familial retinal arterial macroaneurysm
- Familial scaphocephaly syndrome, McGillivray type
- Familial sick sinus syndrome
- Familial spontaneous pneumothorax
- Familial steroid-resistant nephrotic syndrome with sensorineural deafness
- Familial thoracic aortic aneurysm and aortic dissection
- Familial thrombocytosis
- Familial thrombomodulin anomalies
- Familial thyroglossal duct cyst
- Familial thyroid dyshormonogenesis
- Familial tumoral calcinosis
- Familial type 3 hyperlipoproteinemia
- Familial type 5 hyperlipoproteinemia
- Familial ventricular tachycardia
- Familial vesicoureteral reflux
- Familial visceral amyloidosis, Ostertag type
- Familial X-linked hypophosphatemic vitamin D refractory rickets
- Fanconi anemia
- Fanconi anemia complementation group D1
- Fanconi-Bickel syndrome
- Farber lipogranulomatosis
- Farmers lung
- Fasciitis with eosinophilia syndrome
- FASTKD2-related infantile mitochondrial encephalomyopathy
- Fatal familial insomnia
- Fatal infantile encephalocardiomyopathy
- Fatal infantile hypertonic myofibrillar myopathy
- Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
- Fatal multiple mitochondrial dysfunctions syndrome
- Fatal post-viral neurodegenerative disorder
- Fatty acid hydroxylase-associated neurodegeneration
- Fatty acyl-CoA reductase 1 deficiency
- FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome
- Febrile infection-related epilepsy syndrome
- Febrile ulceronecrotic Mucha-Habermann disease
- Feingold syndrome
- Feingold syndrome type 1
- Felty syndrome
- Female infertility due to oocyte meiotic arrest
- Female infertility due to zona pellucida defect
- Femoral hypoplasia - unusual facies syndrome
- Femur-fibula-ulna complex
- Ferro-cerebro-cutaneous syndrome
- Fetal akinesia deformation sequence
- Fetal akinesia syndrome, X-linked
- Fetal akinesia-cerebral and retinal hemorrhage syndrome
- Fetal and neonatal alloimmune thrombocytopenia
- Fetal cytomegalovirus syndrome
- Fetal enterovirus syndrome
- Fetal iodine syndrome
- Fetal methylmercury syndrome
- Fetal parainfluenza virus type 3 syndrome
- Fetal parvovirus syndrome
- FG syndrome 1
- Fibrochondrogenesis
- Fibrolamellar hepatocellular carcinoma
- Fibromatosis, gingival, 1
- Fibromatosis, gingival, 2
- Fibromatosis, gingival, 3
- Fibromatosis, gingival, 4
- Fibronectin glomerulopathy
- Fibrosarcoma
- Fibrous dysplasia
- Fibrous dysplasia of jaw
- Fibular aplasia-ectrodactyly syndrome
- Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome
- Fibular dimelia-diplopodia syndrome
- Fibular hemimelia
- Fibulo-ulnar hypoplasia-renal anomalies syndrome
- Filarial elephantiasis
- Filippi syndrome
- Fine-Lubinsky syndrome
- Finger clinodactyly
- Finger hyperphalangy - toe anomalies - severe pectus excavatum syndrome
- Fingerprint body myopathy
- Finnish congenital nephrotic syndrome
- Finnish type amyloidosis
- Finnish upper limb-onset distal myopathy
- Fish-eye disease
- Flat face-microstomia-ear anomaly syndrome
- Fleck corneal dystrophy
- Floating-Harbor syndrome
- Florid cemento-osseous dysplasia
- FLOTCH syndrome
- Flynn-Aird syndrome
- FMF
- Focal acral hyperkeratosis
- Focal dermal hypoplasia
- Focal epilepsy-intellectual disability-cerebro-cerebellar malformation
- Focal facial dermal dysplasia
- Focal facial dermal dysplasia type III
- Focal palmoplantar and gingival keratoderma
- Focal palmoplantar keratoderma with joint keratoses
- Foix chavany Marie syndrome
- Folinic acid-responsive seizures
- Follicular atrophoderma and basal cell epitheliomata
- Follicular ichthyosis
- Follicular lymphoma
- Folliculitis decalvans
- Fontaine progeroid syndrome
- Fountain syndrome
- Four X syndrome
- Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
- Foveal hypoplasia-presenile cataract syndrome
- Fowler syndrome
- FOXG1 disorder
- Fragile X syndrome
- Fragile X-associated tremor/ataxia syndrome
- Franceschini Vardeu Guala syndrome
- Francois syndrome
- Frank-Ter Haar syndrome
- Frasier syndrome
- FRAXE
- FRAXF syndrome
- Free sialic acid storage disease
- Freeman-Sheldon syndrome
- Freiberg disease
- Frias syndrome
- Fried syndrome
- Friedreich ataxia
- Frontal fibrosing alopecia
- Frontometaphyseal dysplasia
- Frontonasal dysplasia
- Frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome
- Frontonasal dysplasia with alopecia and genital anomaly
- Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome
- Frontorhiny
- Frontotemporal dementia
- Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
- Frontotemporal dementia and/or amyotrophic lateral sclerosis 7
- Frontotemporal dementia with motor neuron disease
- Fructose-biphosphatase deficiency
- Fryns Smeets Thiry syndrome
- Fryns syndrome
- FSGS
- Fuchs heterochromic iridocyclitis
- Fuchs' endothelial dystrophy
- Fucosidosis
- Fuhrmann syndrome
- Fukuda-Miyanomae-Nakata syndrome
- Fumarase deficiency
- Fundus dystrophy, pseudoinflammatory, recessive form
- Fundus pulverulentus
- Fungal meningitis
- Furuncular myiasis
- Fusariosis
- Fused mandibular incisors
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