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Disease	Synonyms	Description	Articles
tinea barbae	dermatophytosis of beard	A dermatophytosis that results_in fungal infection..[+] A dermatophytosis that results_in fungal infection which effects horny layer of epidermis of the bearded areas located_in face or located_in neck, has_material_basis_in Trichophyton mentagrophytes or has_material_basis_in Trichophyton verrucosum, which also effects hair, and effects nail and has_symptom inflammatory kerion-like plaques, and results_in_formation_of noninflammatory superficial perifollicular pustules. [-]
tinea imbricata		A tinea corporis that results_in fungal infection ..[+] A tinea corporis that results_in fungal infection located_in skin, has_material_basis_in Trichophyton concentricum, which is characterized by ring-like growth in overlapping circles that may have an autosomal dominant genetic predisposition. [-]
tuberculous salpingitis		An urogenital tuberculosis that results_in formati..[+] An urogenital tuberculosis that results_in formation of granulomas located_in fallopian tube. [-]
tick-borne encephalitis	Taiga encephalitis; Russian spring-summer encephal.. [+] Taiga encephalitis; Russian spring-summer encephalitis; Siberian tick-borne encephalitis; west-Siberian encephalitis; Western European tick-borne encephalitis; Central European encephalitis; Far Eastern TBE [-]	A viral infectious disease that results_in inflamm..[+] A viral infectious disease that results_in inflammation located_in brain, has_material_basis_in Tick-borne encephalitis virus, which is transmitted_by Ixodes ticks. The infection has_symptom drowsiness, has_symptom confusion, has_symptom sensory disturbances, and has_symptom paralysis. [-]
thelaziasis		A parasitic helminthiasis infectious diseasea that..[+] A parasitic helminthiasis infectious diseasea that involves infection of the eyes in humans by nematode Thelazia callipaeda causing varying degrees of inflammation and lacrimation. In heavier infections, photophobia, edema, conjunctivitis, and blindness occurs. [-]
tungiasis		A parasitic ectoparasitic infectious disease that ..[+] A parasitic ectoparasitic infectious disease that is an inflammatory skin disease caused by the parasitic infestation of the female chigoe flea, Tunga penetrans in animals and humans. The symptoms include skin inflammation, severe pain, itching, and a lesion at the site of infection that is characterized by a black dot at the center of a swollen red lesion, surrounded a white halo. [-]
Trichomonas vaginalis trichomoniasis	urogenital trichomonas	A trichomoniasis that involves infection of the ur..[+] A trichomoniasis that involves infection of the urogenital tract, has_material_basis_in Trichomonas vaginalis, which is transmitted through sexual contact. Symptoms include inflammation of the cervix, urethra and vagina which produce an itching or burning sensation, and yellow-green, itchy, frothy foul-smelling vaginal discharge. [-]
Trichomonas tenax trichomoniasis		A trichomoniasis that is caused by a singled-celle..[+] A trichomoniasis that is caused by a singled-celled protozoan parasite Trichomonas tenax, which is transmitted through oral droplets, by kissing, or on fomites such as eating utensils. Trichomonas tenax causes periodonitis and bronchopulmonary trichomoniasis by aspiration from the oropharynx. [-]
trichosporonosis		An opportunistic mycosis that results_in dissemina..[+] An opportunistic mycosis that results_in disseminated infection, has_material_basis_in Trichosporon and results_in_formation_of nontender erythematous nodules anywhere on the body. [-]
typhoidal tularemia		A tularemia that results_in bacteremia and has_sym..[+] A tularemia that results_in bacteremia and has_symptom fever, has_symptom chills, has_symptom myalgia, has_symptom malaise, and has_symptom weight loss. [-]
trichotillomania		An impulse control disorder that involves the unco..[+] An impulse control disorder that involves the uncontrollable plucking of ones hair. [-]
tooth agenesis	hypodontia; oligodontia; selective tooth agenesis; .. [+] hypodontia; oligodontia; selective tooth agenesis; familial tooth agenesis [-]	A tooth disease characterized by failure to develo..[+] A tooth disease characterized by failure to develop one or more missing teeth. [-]	1 articles
taeniasis	Taenia saginata infectious disease; Infection by T.. [+] Taenia saginata infectious disease; Infection by Taeniarhynchus saginatus; Beef tapeworm infection [-]	A parasitic helminthiasis infectious disease that ..[+] A parasitic helminthiasis infectious disease that has_material_basis_in Taenia solium or has_material_basis_in Taenia saginata, which are transmitted by ingestion of undercooked contaminated meat. [-]
triple-A syndrome	Achalasia-Addisonianism-Alacrimia syndrome; Allgro.. [+] Achalasia-Addisonianism-Alacrimia syndrome; Allgrove Syndrome; AAAS [-]	A syndrome characterized by achalasia, adrenal ins..[+] A syndrome characterized by achalasia, adrenal insufficiency and alacrima and has_material_basis_in mutations in the AAAS gene that encodes ALADIN within the nuclear envelope and results in dysfunction of the autonomic nervous system. [-]
transthyretin amyloidosis	TTR amyloidosis; transthyretin-related hereditary .. [+] TTR amyloidosis; transthyretin-related hereditary amyloidosis; Amyloidosis, hereditary, transthyretin-related; familial amyloid polyneuropathy; Familial transthyretin amyloidosis; paramyloidosis; Corino de Andrade's disease; ATTR amyloidosis; ATTRm amyloidosis [-]	An amyloidosis that is characterized by a loss of ..[+] An amyloidosis that is characterized by a loss of sensation in the extremities, cardiomyopathy, nephropathy, vitreous opacities, and CNS amyloidosis resulting from abnormal deposits of amyloid protein in the body's organs and tissues and has_material_basis_in autosomal dominant inheritance of mutations in the TTR gene. [-]
tyrosinemia type II	Oculocutaneous tyrosinemia; Richner-Hanhart syndro.. [+] Oculocutaneous tyrosinemia; Richner-Hanhart syndrome [-]	A tyrosinemia that has_material_basis_in deficienc..[+] A tyrosinemia that has_material_basis_in deficiency of hepatic tyrosine aminotransferase located_in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels. [-]
tyrosinemia type I	hepatorenal tyrosinemia	A tyrosinemia that has_material_basis_in deficienc..[+] A tyrosinemia that has_material_basis_in deficiency of the enzyme fumarylacetoacetate hydrolase resulting in an increase in fumarylacetoacetate which inhibits previous steps in tyrosine degradation leading to an accumulation of tyrosine in the body. [-]
tyrosinemia type III		A tyrosinemia that has_material_basis_in deficienc..[+] A tyrosinemia that has_material_basis_in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine. [-]
T-cell large granular lymphocyte leukemia	T-cell large granular lymphocyte leukaemia; Large .. [+] T-cell large granular lymphocyte leukaemia; Large granular lymphocytic leukemia; Large granular lymphocytic leukaemia [-]	A T-cell acute lymphocytic leukemia that exhibits ..[+] A T-cell acute lymphocytic leukemia that exhibits an unexplained, chronic (greater than 6 months) elevation in large granular lymphocytes (LGLs) in the peripheral blood. [-]
tarsal-carpal coalition syndrome		A dysostosis that is characterized by fusion of th..[+] A dysostosis that is characterized by fusion of the carpals, tarsals, and phalanges, short first metacarpals causing brachydactyly; and humeroradial fusion. [-]
temtamy preaxial brachydactyly syndrome	PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE	A syndrome that is characterized by brachydactyly,..[+] A syndrome that is characterized by brachydactyly, hyperphalangism of digits, facial dysmorphism, dental anomalies, sensorineural hearing loss, delayed motor and mental development, and growth retardation and has_material_basis_in homozygous mutation in the CHSY1 gene. [-]
transcobalamin II deficiency	TCN2 deficiency	A vitamin B12 deficiency that is characterized by ..[+] A vitamin B12 deficiency that is characterized by a lack of vitamin B12 intestinal absorption resulting from a deficiency in the B12 transport protein TCII. [-]
third-degree atrioventricular block	complete AV block	n_a
tricuspid valve disease	Tricuspid disease; disease of tricuspid valve; RH... [+] Tricuspid disease; disease of tricuspid valve; RH. tricuspid valve disease; Rheumatic disease of tricuspid valve (disorder); rheumatic tricuspid valve disease; Rheumatic tricuspid valve disease NOS (disorder); Rheumatic tricuspid valve disease; Rheumatic disease of tricuspid valve [-]	A heart valve disease that is characterized by val..[+] A heart valve disease that is characterized by valvular insufficiency or valvular stenosis, located_in tricuspid valve between the right atrium and right ventricle. [-]
tongue squamous cell carcinoma		A head and neck squamous cell carcinoma that is lo..[+] A head and neck squamous cell carcinoma that is located_in the tongue. [-]
triosephosphate isomerase deficiency	Triose phosphate-isomerase deficiency	A glucose metabolism disorder that is characterize..[+] A glucose metabolism disorder that is characterized by chronic haemolytic anaemia, cardiomyopathy, susceptibility to infections and severe neurological dysfunction, and has_material_basis_in the triosephosphate isomerase enzyme (TPI1) gene inherited as an autosomal recessive trait. [-]
Troyer syndrome	autosomal recessive spastic paraplegia 20; autosom.. [+] autosomal recessive spastic paraplegia 20; autosomal recessive spastic paraplegia Troyer type; autosomal recessive spastic paraplegia type 20; childhood-onset spastic paraparesis with distal muscle wasting; hereditary spastic paraplegia 20; spastic paraplegia 20 (Troyer syndrome); spastic paraplegia type 20; SPG20; spastic paraplegia 20 [-]	A hereditary spastic paraplegia that is characteri..[+] A hereditary spastic paraplegia that is characterized by spasticity of the leg muscles, progressive muscle weakness, paraplegia, muscle wasting in the hands and feet (distal amyotrophy), small stature, developmental delay, learning disorders, speech difficulties (dysarthria), and mood swings, and has_material_basis_in a mutation of the SPG20 gene. [-]
Townes-Brocks syndrome		A syndrome that is characterized by imperforate an..[+] A syndrome that is characterized by imperforate anus, dysplastic ears often associated with sensorineural and/or conductive hearing impairment, and thumb malformations. [-]	2 articles
trachea mucoepidermoid carcinoma		A mucoepidermoid carcinoma located_in the trachea.
tonsil squamous cell carcinoma		A tonsil cancer that has_material_basis_in squamou..[+] A tonsil cancer that has_material_basis_in squamous cells. [-]
triple-receptor negative breast cancer		A breast cancer that is characterized by the absen..[+] A breast cancer that is characterized by the absence of estrogen, progresterone and Her2 receptors. [-]
thoracic benign neoplasm		An organ system benign neoplam that is located_in ..[+] An organ system benign neoplam that is located_in the thoracic cavity. [-]
thoracic disease		A disease of anatomical entity that is located_in ..[+] A disease of anatomical entity that is located_in the thoracic cavity. [-]	13 articles
tactile agnosia		An agnosia that is a loss of the ability to recogn..[+] An agnosia that is a loss of the ability to recognize or identify objects by touch alone. [-]
time agnosia		An agnosia that is a loss of the ability to compre..[+] An agnosia that is a loss of the ability to comprehend the succession and duration of events. [-]
topographical agnosia		An agnosia that is a loss of the ability to rely o..[+] An agnosia that is a loss of the ability to rely on visual cues to guide them directionally due to the inability to recognise objects. [-]
Timothy syndrome		A syndrome that is characterized by cardiac, hand/..[+] A syndrome that is characterized by cardiac, hand/foot, facial, and neurodevelopmental features. The two forms are type 1 (classic) and type 2, a rare form that has_material_basis_in mutations in a transcript variant of the CACNA1C gene on chromosome 12p13.33. [-]	3 articles
type I complement component 8 deficiency		n_a
type II complement component 8 deficiency		n_a
tracheomalacia	congenital tracheomalacia	A tracheal disease characterized by flaccidity of ..[+] A tracheal disease characterized by flaccidity of the tracheal support cartilage. [-]
transient neonatal diabetes mellitus		A neonatal diabetes that is characterized by hyper..[+] A neonatal diabetes that is characterized by hyperglycemia during the neonatal period that remits during infancy but recurs in later life in most patients. [-]	1 articles
Thiel-Behnke corneal dystrophy	TBCD; corneal dystrophy honeycomb-shaped; Waardenb.. [+] TBCD; corneal dystrophy honeycomb-shaped; Waardenburg-Jonker corneal dystrophy; corneal dystrophy of Bowman layer type II; anterior limiting membrane dystrophy type II [-]	An epithelial-stromal TGFBI dystrophy that is char..[+] An epithelial-stromal TGFBI dystrophy that is characterized by recurrent erosions and honeycomb-shaped opacification located_in the cornea, proteinaceous deposits in the anterior stroma and subepithelium, and progressive early vision loss, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased protein deposition and disruption especially of Bowman's membrane of the cornea. [-]
Timothy grass allergy		A pollen allergy triggered by Phleum pratense poll..[+] A pollen allergy triggered by Phleum pratense pollen. [-]
tomato allergy	Solanum lycopersicum fruit allergy	A fruit allergy triggered by Solanum lycopersicum ..[+] A fruit allergy triggered by Solanum lycopersicum plant fruit food product. [-]
tiger prawn allergy	Penaeus monodon allergy	A crustacean allergy triggered by Penaeus monodon.
torsion dystonia 1	dystonia musculorum deformans	A generalized dystomia characterized by autosomal ..[+] A generalized dystomia characterized by autosomal dominant inheritance of dystonia usually presenting initially as focal, typically in the limbs, but often generalizes with age that has_material_basis_in heterozygous mutation in the TOR1A gene on chromosome 9q34. [-]
T-cell immunodeficiency, congenital alopecia, and nail dystrophy	winged helix deficiency; alymphoid cystic thymic d.. [+] winged helix deficiency; alymphoid cystic thymic dysgenesis; severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome [-]	A severe combined immunodeficiency characterized b..[+] A severe combined immunodeficiency characterized by congenital alopecia, severe T-cell immunodeficiency, and ridging, pitting or curving of all nails that has_material_basis_in homozygous mutation in the FOXN1 gene on chromosome 17q11-q12. [-]
transient myeloproliferative syndrome	transient leukemia of Down syndrome; transient leu.. [+] transient leukemia of Down syndrome; transient leukemia; transient myeloproliferative disease; transient leurkemia of Down syndrome; transient abnormal myelopoiesis; TAM; MST [-]	A myeloproliferative neoplasm characterized by leu..[+] A myeloproliferative neoplasm characterized by leukocytosis in newborns with Down syndrome. [-]	1 articles
thrombosis		A vascular disease caused by the formation of a bl..[+] A vascular disease caused by the formation of a blood clot inside a blood vessel, obstructing the flow of blood through the circulatory system. [-]
thiamine deficiency disease		A nutritional deficiency disease that is character..[+] A nutritional deficiency disease that is characterized by low levels of thiamine. [-]

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