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Disease	Synonyms	Description	Articles	Phenotypes
focal labyrinthitis	Circumscribed labyrinthitis (disorder); Circumscri.. [+] Circumscribed labyrinthitis (disorder); Circumscribed labyrinthitis [-]	A labyrinthitis which is an infectious inflammator..[+] A labyrinthitis which is an infectious inflammatory disease of a circumscribed area of either the vestibular or the cochlear portion of the labyrinth, or of both together. This is caused by a chronic suppurative otitis media, mastoiditis, or cholesteatoma. [-]
facial paralysis	Facial Palsy	n_a
female breast lower-outer quadrant cancer	malignant neoplasm of lower-outer quadrant of fema.. [+] malignant neoplasm of lower-outer quadrant of female breast (disorder); malignant neoplasm of lower-outer quadrant of female breast [-]	A female breast cancer that is located_in the lowe..[+] A female breast cancer that is located_in the lower-outer qudrant of the breast. [-]
folic acid deficiency anemia	folic acid deficiency anaemia; Folate-deficiency a.. [+] folic acid deficiency anaemia; Folate-deficiency anaemia; Folate deficiency anaemia; Folate-deficiency anemia; Folate-deficient megaloblastic anaemia; Folate deficiency anemia [-]	A nutritional deficiency disease that is character..[+] A nutritional deficiency disease that is characterized by a decrease in red blood cells due to lack of folate, has_material_basis_in insufficient folic acid in diet, hemolytic anemia, alcoholism, and/or certain medicines. [-]
familial lipoprotein lipase deficiency	familial chylomicronemia syndrome; Fredrickson typ.. [+] familial chylomicronemia syndrome; Fredrickson type I hyperlipoproteinemia; familial LPL deficiency; familial chylomiconemia syndrome; Fredrickson type I lipaemia; Fredrickson type I hyperlipoproteinemia (disorder); familial lipoprotein lipase deficiency with type I phenotype; familial lipoprotein lipase deficiency (disorder) [Ambiguous]; familial hyperlipoproteinemia type I; familial hyperchylomicronemia (disorder); hypercholesterinaemic xanthomatosis; hyperchylomicronemia; mixed hyperglyceridemia [-]	A familial hyperlipemia characterized by a deficie..[+] A familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides. [-]
frozen shoulder	Adhesive capsulitis of shoulder; adhesions-capsuli.. [+] Adhesive capsulitis of shoulder; adhesions-capsulitis,shoulder [-]	A connective tissue disease characterized by restr..[+] A connective tissue disease characterized by restriction of both active and passive range of motion located_in the scapulohumeral joint and has_symptom pain and has_symptom restricted range of motion. [-]
fragile X syndrome	FRAGILE X MENTAL RETARDATION SYNDROME; MARTIN-BELL.. [+] FRAGILE X MENTAL RETARDATION SYNDROME; MARTIN-BELL SYNDROME; MARKER X SYNDROME [-]	A syndrome that is characterized by moderate to se..[+] A syndrome that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in X-linked inheritance and a loss of FMR1 function. [-]	4 articles
farmer's lung	Farmers lung; farmer lung	An extrinsic allergic alveolitis which is induced ..[+] An extrinsic allergic alveolitis which is induced by the inhalation of spores (Aspergillus sp and thermophilic actinomycetes) in dust from moldy hay or straw. It is characterized by sudden onset, fever, cough, expectoration, and breathlessness. [-]
Fabry disease	Fabry's disease; Fabry Disease, Cardiac Variant; A.. [+] Fabry Disease, Cardiac Variant; Fabry's disease; Alpha-galactosidase A deficiency; Angiokeratoma Corporis Diffusum; alpha galactosidase deficiency; deficiency of melibiase [-]	A sphingolipidosis that is characterized by the bu..[+] A sphingolipidosis that is characterized by the buildup of globotriaosylceramide in the body's cells and has_material_basis_in X-linked inherited mutations in the GLA gene, encoding alpha-galactosidase A, on chromosome Xq22. [-]
fucosidosis	alpha fucosidase deficiency; A-fucosidase deficien.. [+] alpha fucosidase deficiency; A-fucosidase deficiency [-]	n_a
Foster-Kennedy syndrome		n_a
FG syndrome	Keller syndrome; Opitz-Kaveggia syndrome	A syndrome characterized by retardation, hyperacti..[+] A syndrome characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern. [-]
formaldehyde allergic contact dermatitis	allergic contact dermatitis to formalin	An allergic contact dermatitis that has_allergic_t..[+] An allergic contact dermatitis that has_allergic_trigger formaldehyde. [-]
Far Eastern spotted fever	Rickettsia heilongjiangensis spotted fever	A spotted fever that has_material_basis_in Rickett..[+] A spotted fever that has_material_basis_in Rickettsia heilongjiangensis, which is transmitted_by ticks (Haemaphysalis concinna). The infection has_symptom fever, has_symptom eschar, has_symptom maculopapular rash, and has_symptom regional adenopathy. [-]
Flinders Island spotted fever	FISF; Thai tick typhus	A spotted fever that has_material_basis_in Rickett..[+] A spotted fever that has_material_basis_in Rickettsia honei, which is transmitted_by cayenne ticks (Amblyomma cajennense). The infection has_symptom mild spotted fever, has_symptom eschar and has_symptom adenopathy. [-]
fusariosis		An opportunistic mycosis that involves localized o..[+] An opportunistic mycosis that involves localized or hematogenously disseminated fungal infection by Fusarium solani or Fusarium oxysporum. Skin lesions are seen in neutropenic patients, and indolent cellulitis or soft-tissue necrosis occur in immunocompromised patients at the site of trauma. [-]
foodborne botulism		A botulism that involves intoxication caused by bo..[+] A botulism that involves intoxication caused by botulinum neurotoxins (BoNTA, B, E and F), which are transmitted by ingestion of food contaminated with preformed toxins, has_material_basis_in Clostridium botulinum A, has_material_basis_in Clostridium botulinum B, has_material_basis_in Clostridium botulinum E and has_material_basis_in Clostridium botulinum F. The infection has symptom blurred vision, has symptom diplopia, has symptom dysarthria, has symptom dysphonia, has symptom dysphagia and has symptom descending muscle paralysis. [-]
familial adenomatous polyposis	adenomatous polyposis of the colon	An intestinal disease that has_material_basis_in m..[+] An intestinal disease that has_material_basis_in mutations in the APC gene and involves formation of numerous polyps in the epithelium of the large intestine which are initially benign and later transform into colon cancer. [-]	3 articles
fatal familial insomnia		A prion disease that is characterized by insomnia,..[+] A prion disease that is characterized by insomnia, hallucinations, dementia and death, located_in the brain. [-]
Frasier syndrome		A syndrome that is characterized by gonadal dysgen..[+] A syndrome that is characterized by gonadal dysgenesis, streak gonads, progressive focal segmental glomerulonephropathy and the development of urogenital cancers that is the result of mutation in the WT1 gene. [-]
familial partial lipodystrophy	Koberling-Dunnigan Syndrome; Dunnigan Syndrome	A partial lipodystrophy characterized by abnormal ..[+] A partial lipodystrophy characterized by abnormal subcutaneous adipose tissue distribution beginning in late childhood or early adult life. [-]
Farber lipogranulomatosis	Farber Disease; Farber disease; Acid Ceramidase De.. [+] Farber disease; Farber Disease; Acid Ceramidase Deficiency; N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY; acid ceramidase deficiency; N-laurylsphingosine deacylase deficiency [-]	A lipid storage disease that is characterized by a..[+] A lipid storage disease that is characterized by abnormalities in swallowing, cognition, joint function, and central nervous system due to a deficiency in the enzyme ceramidase that results in sphingolipids deposition. [-]
familial medullary thyroid carcinoma	THYROID CARCINOMA, FAMILIAL MEDULLARY	A thyroid gland medullary carcinoma that has_mater..[+] A thyroid gland medullary carcinoma that has_material_basis_in autosomal dominant inheritance. [-]
Fukuyama congenital muscular dystrophy		A congenital muscular dystrophy-dystroglycanopathy..[+] A congenital muscular dystrophy-dystroglycanopathy type A that is characterized by muscle weakness, failure to thrive, severe intellectual and developmental disability, impaired vision and cardiac abnormalities and has_material_basis_in mutation in the FKTN gene that produces the fukutin protein. [-]
familial visceral amyloidosis	AMYLOIDOSIS, FAMILIAL RENAL; German type amyloidos.. [+] AMYLOIDOSIS, FAMILIAL RENAL; German type amyloidosis; OSTERTAG TYPE AMYLOIDOSIS; systemic nonneuropathic amyloidosis [-]	An amyloidosis that is characterized by the abnorm..[+] An amyloidosis that is characterized by the abnormal deposition of amyloid proteins that is located_in the visceral organs, primarily the kidneys. [-]
Finnish type amyloidosis	AMYLOIDOSIS, MERETOJA TYPE; AGel amyloidosis; gels.. [+] AMYLOIDOSIS, MERETOJA TYPE; AGel amyloidosis; gelsolin amyloidosis; Lattice corneal dystrophy type II [-]	An amyloidosis that is characterized by abnormal d..[+] An amyloidosis that is characterized by abnormal deposits of amyloid protein that mainly affect the eyes, nerves and skin and has_material_basis_in mutations in the gelsolin gene (GSN), and has_symptom corneal lattice dystrophy, has_symptom bilateral facial paralysis, has_symptom cutis laxa. [-]
familial atrial fibrillation	ATFB	An atrial fibrillation that has_material_basis_in ..[+] An atrial fibrillation that has_material_basis_in autosomal dominant inheritance of the familial atrial fibrillation (ATFB) genes. [-]
fetal alcohol syndrome		A fetal alcohol spectrum disorder that results in ..[+] A fetal alcohol spectrum disorder that results in severe mental and physical defects which can develop in a child when the mother drinks alcohol during pregnancy. The presenting features include craniofacial dysmorphology (microcephaly, smooth philtrum, thin upper lip, small eye openings), pre- and postnatal growth deficiency, and central nervous system dysfunction. [-]	10 articles	13 matches
female breast cancer		n_a
fetal alcohol spectrum disorder		A specific developmental disorder and physical dis..[+] A specific developmental disorder and physical disorder that is characterized by physical, behavioral and learning birth defects resulting from maternal ingestion of alcohol during pregnancy. [-]	15 articles	13 matches
funisitis		A connective tissue disease that is an inflammatio..[+] A connective tissue disease that is an inflammation of the connective tissue of the umbilical cord. [-]
fibular hypoplasia and complex brachydactyly	Du Pan syndrome; acromesomelic dysplasia-2B	An acromesomelic dysplasia that is characterized b..[+] An acromesomelic dysplasia that is characterized by severe reduction or absence of the fibula and complex brachydactyly. [-]
first-degree atrioventricular block		n_a
familial encephalopathy with neuroserpin inclusion bodies	FENIB	A neurodegenerative disease that is characterized ..[+] A neurodegenerative disease that is characterized by intraneuronal inclusions of mutant neuroserpin resulting in progressive encephalopathy, dementia and seizures and has_material_basis_in a mutation in the SERPINI1 gene inherited in an in autosomal dominant pattern. [-]
focal dystonia		A dystonia that is localized to a specific part of..[+] A dystonia that is localized to a specific part of the body. [-]	1 articles
focal hand dystonia	organic writer's cramp	A focal dystonia that affects a single muscle or s..[+] A focal dystonia that affects a single muscle or small group of muscles in the hand resulting from involuntary muscular contractions. [-]
fibroma		A connective tissue benign neoplasm composed of fi..[+] A connective tissue benign neoplasm composed of fibrous or connective tissues that derives_from mesenchymal tissue. [-]
follicular lymphoma		A B-cell lymphoma that is characterized as an indo..[+] A B-cell lymphoma that is characterized as an indolent non-Hodgkin's lymphoma and has_material_basis_in follicle center B-cells (centrocytes and centroblasts). [-]
fragile X-associated tremor/ataxia syndrome	FXTAS syndrome	A X-linked hereditary ataxia that is characterized..[+] A X-linked hereditary ataxia that is characterized by adult-onset progressive intention tremor and gait ataxia, has_material_basis_in expanded trinucleotide repeat of the FMR1 gene that results_in a toxic gain of function of FMR1 RNA. [-]	1 articles
familial juvenile hyperuricemic nephropathy		A kidney disease that is characterized by hyperuri..[+] A kidney disease that is characterized by hyperuricemia with renal uric acid under-excretion, gout and chronic kidney disease. [-]	1 articles
female reproductive organ benign neoplasm		n_a
fallopian tube benign neoplasm		n_a
finger agnosia		An agnosia that is a loss of the ability to distin..[+] An agnosia that is a loss of the ability to distinguish the fingers on the hand. [-]
form agnosia		An agnosia that is a loss of the ability to percei..[+] An agnosia that is a loss of the ability to perceive a whole object while perceiving only parts of details. [-]
familial hemiplegic migraine		A migraine with aura that is characterized by temp..[+] A migraine with aura that is characterized by temporary numbness or weakness, often affecting one side of the body (hemiparesis). Additional features of an aura can include difficulty with speech, confusion, and drowsiness. [-]	4 articles
frontotemporal dementia and/or amyotrophic lateral sclerosis 6	ALS14; amyotrophic lateral sclerosis 14; amyotroph.. [+] ALS14; amyotrophic lateral sclerosis 14; amyotrophic lateral sclerosis, with or without frontotemporal dementia; amyotrophic lateral sclerosis type 14 [-]	An amyotrophic lateral sclerosis that has_material..[+] An amyotrophic lateral sclerosis that has_material_basis_in mutation in the VCP gene on chromosome 9p13. [-]
frontotemporal dementia and/or amyotrophic lateral sclerosis 1	FTDMND; FTDALS1; frontotemporal dementia and/or mo.. [+] FTDALS1; FTDMND; frontotemporal dementia and/or motor neuron disease; frontotemporal dementia and/or amyotrophic lateral sclerosis 1; amyotrophic lateral sclerosis and/or frontotemporal dementia; ALSFTD [-]	An amyotrophic lateral sclerosis that has_material..[+] An amyotrophic lateral sclerosis that has_material_basis_in mutation in the C9ORF72 gene on chromosome 9. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis. [-]
frontotemporal dementia and/or amyotrophic lateral sclerosis 2	FTDALS2; frontotemporal dementia and/or amyotrophi.. [+] FTDALS2; frontotemporal dementia and/or amyotrophic lateral sclerosis 2 [-]	An amyotrophic lateral sclerosis that has_material..[+] An amyotrophic lateral sclerosis that has_material_basis_in mutation in the CHCHD10 gene on chromosome 22. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis. [-]
Fleck corneal dystrophy	FCD; Francois-Neetens speckled corneal dystrophy	A stromal dystrophy that is characterized by numer..[+] A stromal dystrophy that is characterized by numerous tiny, dot-like white flecks scattered in all layers of the corneal stroma and that has_material_basis_in heterozygous mutation in the PIKFYVE gene on chromosome 2q34. [-]
Feingold syndrome	FGLDS; digital anomalies with short palpebral fiss.. [+] FGLDS; digital anomalies with short palpebral fissures and atresia of esophagus or duodenum; microcephaly-oculo-digito-esophageal-duodenal syndrome; MODED syndrome; oculo-digito-esophageal-duodenal syndrome; ODED syndrome; microcephaly-digital anomalies-normal intelligence syndrome [-]	A syndrome characterized by variable combinations ..[+] A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation. [-]

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