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Disease	Synonyms	Description
familial hypercholesterolemia	Fredrickson type IIa lipidaemia; Fredrickson type .. [+] Fredrickson type IIa lipidaemia; Fredrickson type IIa hyperlipoproteinemia; familial hypercholesteremia; familial hyperbetalipoproteinaemia; hyperbetalipoproteinemia; type II hyperlipidemia [-]	A familial hyperlipidemia characterized by very hi..[+] A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. [-]
facial neuralgia		n_a
focal labyrinthitis	Circumscribed labyrinthitis; Circumscribed labyrin.. [+] Circumscribed labyrinthitis; Circumscribed labyrinthitis (disorder) [-]	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) [-]	n_a
folic acid deficiency anemia	Folate-deficient megaloblastic anaemia; Folate-def.. [+] Folate-deficient megaloblastic anaemia; Folate-deficiency anemia; Folate deficiency anemia [-]	n_a
familial lipoprotein lipase deficiency	Fredrickson type I hyperlipoproteinemia; familial .. [+] Fredrickson type I hyperlipoproteinemia; familial chylomiconemia syndrome; Fredrickson type I lipaemia; Fredrickson type I hyperlipoproteinemia (disorder); familial LPL deficiency; 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	adhesions-capsulitis,shoulder; Adhesive capsulitis.. [+] adhesions-capsulitis,shoulder; Adhesive capsulitis of shoulder [-]	n_a
fragile X syndrome	FRAGILE X MENTAL RETARDATION SYNDROME; MARKER X SY.. [+] FRAGILE X MENTAL RETARDATION SYNDROME; MARKER X SYNDROME; MARTIN-BELL 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. [-]
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; alpha galactosidase deficiency; A.. [+] Fabry's disease; alpha galactosidase deficiency; Alpha-galactosidase A deficiency; Angiokeratoma Corporis Diffusum; deficiency of melibiase [-]	n_a
fucosidosis	A-fucosidase deficiency; alpha fucosidase deficien.. [+] A-fucosidase deficiency; alpha fucosidase deficiency [-]	n_a
Foster-Kennedy syndrome		n_a
FG syndrome	Keller syndrome; Opitz-Kaveggia syndrome	An X-linked disease characterized by retardation, ..[+] An X-linked disease 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. [-]
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 autosomal dominant disease that is has material..[+] An autosomal dominant disease that is 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. [-]
fatal familial insomnia		n_a
Frasier syndrome		n_a
familial partial lipodystrophy	Dunnigan Syndrome; Koberling-Dunnigan Syndrome	A lipodystrophy characterized by abnormal subcutan..[+] A 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 medullary carcinoma that has_material_ba..[+] A thyroid medullary carcinoma that has_material_basis_in autosomal dominant inheritance. [-]
Fukuyama congenital muscular dystrophy		n_a
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	n_a
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. [-]
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. [-]
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. [-]
fatal infantile encephalocardiomyopathy	fatal infantile COX deficiency; fatal infantile ca.. [+] fatal infantile COX deficiency; fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency; cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency [-]	A mitochondrial metabolism disease that has_materi..[+] A mitochondrial metabolism disease that has_material_basis_in a mutation in the SCO2 gene which encodes a COX assembly factor and results in deficiency of cytochrome c oxidase. [-]
fibular hypoplasia and complex brachydactyly	Du Pan syndrome	An autosomal recessive disease that is characteris..[+] An autosomal recessive disease that is characterised 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. [-]
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. [-]
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. [-]
female reproductive organ benign neoplasm		A reproductive organ benign neoplasm that is chara..[+] A reproductive organ benign neoplasm that is characterized by a lack of malignancy located_in the female reproductive system. [-]
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. [-]
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; ALSFTD; amyotrophic lateral sclerosis and/or frontotemporal dementia [-]	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. [-]
FTDALS2	frontotemporal dementia and/or amyotrophic lateral.. [+] 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	Francois-Neetens speckled corneal dystrophy; FCD	n_a

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