Conditions
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T2-High AsthmaA chronic asthma that is characterized by the pathophysiology phenotype combination (endotype) of early-onset allergic asthma, late-onset eosinophilic asthma, and aspirin-exacerbated respiratory disease.T2-Low AsthmaA chronic asthma that is characterized by the pathophysiology phenotype combination (endotype) of non-atopic, smoking, obesity related, and elderly and that is characterized by neutrophilic (sputum neutrophils > 40–60%)Tabes DorsalisA tertiary neurosyphilis that results in slow degeneration of the nerve cells and nerve fibers that carry sensory information to the brain. The infection has symptom intense, stabbing pain in the back and legs that recurTachycardiaAn unusually fast resting heart rate.Tactile AgnosiaAn agnosia that is a loss of the ability to recognize or identify objects by touch alone.TaeniasisA parasitic helminthiasis infectious disease that is caused by Taenia solium or is caused by Taenia saginata, which are transmitted by ingestion of undercooked contaminated meat.Takayasu ArteritisInflammation of the aorta and its major branches.Takayasu'S ArteritisA vasculitis that involves inflammation of the aorta that carries blood from the heart to the rest of the body.Tall Cell Papillary Thyroid CarcinomaA papillary thyroid carcinoma that is characterized by the presence of tall malignant follicular cells, arranged in papillary and trabecular patterns.Tamoxifen-Related Endometrial LesionAn endometrial disease that is caused by tamoxifen exposure.Tangier DiseaseA hypolipoproteinemia that is characterized by markedly reduced levels of plasma high density lipoproteins resulting in tissue accumulation of cholesterol esters and that is caused by homozygous or compound heterozygousTANGO2-Related Metabolic Encephalopathy and ArrythmiasA syndrome that is characterized by episodic metabolic degeneration affecting skeletal muscle, cardiac muscle, and the nervous system and that is caused by homozygous or compound heterozygous mutation in the TANGO2 geneTapewormA parasitic worm infection from undercooked meat.Tardive DyskinesiaInvoluntary movements from long-term medication use.TARP SyndromeA syndrome characterized by talipes equinovarus, atrial septal defect, Robin sequence (micrognathia, cleft palate, and glossoptosis), and persistent left superior vena cava typically resulting in late prenatal or early pTarsal-Carpal Coalition SyndromeA dysostosis that is characterized by fusion of the carpals, tarsals, and phalanges, short first metacarpals causing brachydactyly; and humeroradial fusion.Tarsal Tunnel SyndromeNerve compression in the ankle.Tatton-Brown-Rahman SyndromeA syndromic intellectual disability characterized by tall stature, a distinctive facial appearance, and impaired intellectual development that is caused by heterozygous mutation in the DNMT3A gene on chromosome 2p23.3.TauopathyA neurodegenerative disease that is caused by the pathological aggregation of tau protein in so-called neurofibrillary tangles (NFT) in the human brain.Tay-Sachs DiseaseA rare inherited disorder that destroys nerve cells.T-Cell Acute Lymphoblastic LeukemiaAn acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood.T-Cell Adult Acute Lymphocytic LeukemiaAn adult acute lymphocytic leukemia occurring in adults and that is caused by T cells.T Cell and NK Cell ImmunodeficiencyA primary immunodeficiency disease that involves multiple components of the immune system, including both T cell and NK cell immunodeficiency.T Cell, B Cell, and NK Cell DeficiencyA combined immunodeficiency characterized by impaired function or reduced numbers of T cells, B cells, and natural killer (NK) cells.T-Cell Childhood Lymphoblastic LymphomaA lymphoblastic lymphoma that is caused by T-cells and that occurs during childhood.T Cell DeficiencyA primary immunodeficiency disease that is characterized by decreased numbers of circulating or functioning T cells.T-Cell Immunodeficiency, Congenital Alopecia, and Nail DystrophyA severe combined immunodeficiency characterized by congenital alopecia, severe T-cell immunodeficiency, and ridging, pitting or curving of all nails that is caused by homozygous mutation in the FOXN1 gene on chromosomeT-Cell Large Granular Lymphocyte LeukemiaA T-cell acute lymphocytic leukemia that exhibits an unexplained, chronic (greater than 6 months) elevation in large granular lymphocytes (LGLs) in the peripheral blood.T-Cell Non-Hodgkin LymphomaA non-Hodgkin lymphoma of T-cell lineage.T-Cell Prolymphocytic LeukemiaA prolymphocytic leukemia that is characterized by the proliferation of small to medium sized prolymphocytes with a mature T-cell phenotype, involving the blood, bone marrow, lymph nodes, liver, spleen, and skin.Teebi Hypertelorism SyndromeA syndrome characterized by hypertelorism, prominent forehead, thick eyebrows, and short nose with broad and depressed features.Teebi Hypertelorism Syndrome 1A Teebi hypertelorism syndrome that is caused by mutation in heterozygous mutation in the SPECC1L gene on chromosome 22q11.2 or heterozygous deletion at chromosome 22q11.2.Teebi Hypertelorism Syndrome 2A Teebi hypertelorism syndrome that is caused by mutation in heterozygous mutation in the CDH11 gene on chromosome 16q21.Telomere Biology DisorderA genetic disease that is characterized by telomeres that are longer or shorter than usual.Temple SyndromeA syndrome characterized by low birth weight, hypotonia and motor delay, feeding problems early in life, early puberty, and significantly reduced final height that is caused by heterozygous mutation in an impriniting regTemporal ArteritisA central nervous system vasculitis that is characterized by inflammation of the lining of arteries, often arteries in the head.Temporal Lobe EpilepsyA common focal epilepsy affecting the temporal lobe.Temporomandibular Joint DisorderPain and dysfunction in the jaw joint.Temtamy Preaxial Brachydactyly SyndromeA 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 is caused bTemtamy SyndromeA syndrome characterized by variable craniofacial dysmorphism, ocular coloboma, seizures, and brain abnormalities including partial or complete absence of the corpus callosum that is caused by [zygosity of] mutation in tTendinitisInflammation of a tendon. Tracking your symptoms and connecting with others who understand can help you manage day to day.Tendon Sheath LipomaA synovium neoplasm that is in the tendon sheath.TenosynovitisAn arthropathy that is characterized as an inflammation of the lining of the sheath that surrounds a tendon.Tenosynovitis of Foot and AnkleA tenosynovitis that is located in the foot and ankle.TeratocarcinomaA mixed germ cell tumor that is a mixture of teratoma with embryonal carcinoma, or with choriocarcinoma, or with both.TeratomaA germ cell and embryonal cancer that is an encapsulated tumor with tissue or organ components resembling normal derivatives of all three germ layers.Teratoma with Somatic-Type MalignancyA teratoma that is characterized by morphologic transformation to malignancy and an aggressive clinical course.Terminal Osseous DysplasiaA syndrome characterized by skeletal dysplasia of the limbs, pigmentary defects of the skin, and recurrent digital fibroma during infancy that is caused by heterozygous mutation in the FLNA gene on chromosome Xq28.Tertiary NeurosyphilisA tertiary syphilis that results in infection located in brain or located in spinal cord.Tertiary SyphilisA syphilis that is characterized as the third stage of syphilis that develops after the disappearance of the secondary symptoms and is marked by ulcers and gummas under the skin and commonly by involvement of the skeletaTesticular Brenner TumorA testicular cancer that is caused by the surface epithelium of the testis and is characterized by the presence of cysts lined by transitional cells and solid nests of transitional cells in a spindle cell stroma.Testicular CancerCancer of the testicles.Testicular Germ Cell CancerA testicular cancer that is caused by germ cells.Testicular Monophasic ChoriocarcinomaA choriocarcinoma of the testis that is characterized by a composition of only cytotrophoblasts and absent syncytiotrophoblastic giant cells.Testicular Non-Seminomatous Germ Cell CancerA testicular malignant germ cell cancer that is characterized by the absence of a seminomatous component.Testicular Sex Cord-Stromal Benign NeoplasmA sex cord-stromal benign neoplasm that arises from the testis.Testicular Sex Cord-Stromal NeoplasmA sex cord-gonadal stromal tumor that is in the testis.Testis RhabdomyosarcomaA testis sarcoma that arises from mesenchymal cells and is in the testis.Testis SarcomaA sarcoma and malignant neoplasm of testis that is in the testis.Tetanic CataractA cataract resulting from hypocalcemia.TetanusA bacterial infection causing painful muscle spasms.Tetanus NeonatorumA tetanus that occurs in newborn babies when the birth cord stump gets dirty through cutting it with an unclean blade or applying substances containing bacteria to it. The infection has symptom stiff body, has symptom muTetraamelia SyndromeA syndrome characterized by rudimentary or absent appendages and anomalies involving the cranium and face, urogenital system, anorectum, heart, lungs, skeleton, and/or central nervous system.Tetraamelia Syndrome 1A tetraamelia syndrome characterized by complete limb agenesis without defects of scapulae or clavicles that is caused by homozygous or compound heterozygous mutation in WNT3 on chromosome 17q21.31-q21.32.Tetraamelia Syndrome 2A tetraamelia syndrome characterized by rudimentary or absent appendages, bilateral agenesis of the lungs, pulmonary vascular abnormalities, and dysmorphic features that is caused by homozygous or compound heterozygous mTetrachlorophthalic Anhydride Allergic AsthmaAn allergic asthma that triggered by tetrachlorophthalic anhydride.Tetrahydrobiopterin (BH4)-Deficient HyperphenylalaninemiaAn amino acid metabolic disorder that are characterized phenotypically by hyperphenylalaninemia, depletion of the neurotransmitters dopamine and serotonin, and progressive cognitive and motor deficits and that is causedTFE3-Rearranged Renal Cell CarcinomaA renal cell carcinoma with MiT translocations that is characterized by the presence of different translocations involving the chromosome Xp11.2 and that result in the creation of gene fusions involving the TFE3 gene.TFEB-Rearranged Renal Cell CarcinomaA renal cell carcinoma with MiT translocations that is characterized by the presence of the chromosomal translocation t(6;11) which fuses the TFEB transcription factor gene, located on chromosome 6, with the MALAT1 gene,Thalamic DiseaseA brain disease that is characterized by Dejerine-Roussy syndrome that develops from thalamic injury.ThalassemiaAn inherited blood disorder that reduces hemoglobin production. Tracking your symptoms and connecting with others who understand can help you manage day to day.Thalassemia MinorA beta thalassemia that is caused by one HBB gene mutation without typical thalassemia symptoms, but may have some symptoms of anemia.Thanatophoric DysplasiaAn osteochondrodysplasia that causes short arms and legs with excess folds of skin.TheileriasisA parasitic protozoa infectious disease that involves infection of humans and cattle caused by a genus of parasitic protozoa Theileria, which is transmitted by ixodid ticks.ThelaziasisA 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, edeThiamine Deficiency DiseaseA nutritional deficiency disease that is characterized by low levels of thiamine.Thiamine-Responsive Megaloblastic Anemia SyndromeA syndrome that is characterized by megaloblastic anemia, non-type I diabetes mellitus, and sensorineural deafness where the anemia and sometimes diabetes is repsonsive to high doses of thiamine, and that is caused by hoThiel-Behnke Corneal DystrophyAn epithelial-stromal TGFBI dystrophy that is characterized by recurrent erosions and honeycomb-shaped opacification in the cornea, proteinaceous deposits in the anterior stroma and subepithelium, and progressive early vThiopental AllergyA drug allergy that triggered by thiopental.Third-Degree Atrioventricular BlockAn atrioventricular block that is characterized by bradycardia, hypotension, hemodynamic instability and complete dissociation between P waves and QRS complexes on electrocardiogram caused when conduction fails to propagThomsen DiseaseA myotonia congenita that is characterized by muscle stiffness and an inability of the muscle to relax after voluntary contraction and that is caused by heterozygous mutation in the gene encoding skeletal muscle chlorideThoracic Aortic AneurysmAn aortic aneurysm that is in the thoracic aorta.Thoracic Benign NeoplasmAn organ system benign neoplam that is in the thoracic cavity.Thoracic CancerAn organ system cancer in the thoracic cavity that develops in the different types of cells within the lungs, as well as less common cancers of the esophagus, the trachea, or the chest wall.Thoracic DiseaseA disease of anatomical entity that is in the thoracic cavity.Thoracic Outlet SyndromeA vascular disease that is characterized by compression at the superior thoracic outlet[1] resulting from excess pressure placed on a neurovascular bundle passing between the anterior scalene and middle scalene muscles.Throat CancerCancer of the throat.ThrombocytopeniaA low platelet count that increases bleeding risk.Thrombocytopenia-Absent Radius SyndromeA chromosomal deletion syndrome that is characterized by absence of the radius bone and platelet deficiency and bilateral absence of the radii with the presence of both thumbs and generally transient thrombocytopenia (leThrombocytosisAn abnormally high platelet count.ThrombophiliaA blood coagulation disease that is characterized by an increased tendency to form clots.Thrombophilia Due to Activated Protein C ResistanceA thrombophilia characterized by resistance of F5 to cleavage and inactivation and increased tendency for thrombosis that is caused by heterozygous mutation in F5 on chromosome 1q24.2.Thrombophilia Due to Decreased Release of PLATA thrombophilia characterized by impaired capacity for release of fibrinolytic activity from the blood vessel walls.Thrombophilia Due to HRG DeficiencyA thrombophilia characterized by decreased histidine-rich glycoprotein (HRG) plasma levels and a tendency to develop thrombosis that is caused by heterozygous mutation in HRG on chromosome 3q27.3.Thrombophilia Due to Thrombin DefectA thrombophilia characterized by recurrent thrombophilia that is caused by heterozygous mutation in F2 on chromosome 11p11.2.Thrombophilia Due to Thrombomodulin DefectA thrombophilia characterized by increased risk of developing arterial but not venous thrombosis that is caused by mutation in the THBD gene on chromosome 20p11.21.ThrombophlebitisA phlebitis that results from a blood clot in the vessel.Thrombophlebitis MigransA thrombophlebitis that is characterized by repeated occurances of thrombophlebitis in different locations.ThrombosisA vascular disease caused by the formation of a blood clot inside a blood vessel, obstructing the flow of blood through the circulatory system.Thunderstorm Triggered AsthmaAn allergic asthma that is characterized by acute asthma attacks immediately following a thunderstorm resulting from inhalation of high concentrations of aeroallergens, most commonly grass pollen.Thymic CarcinomaA thymus cancer that arises from epithelial cells. The tumor cells in a thymic carcinoma look very different from the normal cells of the thymus, grow more quickly, and have usually spread to other parts of the body whenThymomaA thymus cancer that arises from epithelial cells in the thymus. The tumor cells in a thymoma look similar to the normal cells of the thymus, grow slowly, and rarely spread beyond the thymus.Thymoma Type BA thymoma that is an epithelial neoplasm arising from the thymus. It may be associated with myasthenia gravis, pure red cell aplasia, and hypogammaglobulinemia.Thymoma Type B2A thymoma type B that is characterized by the presence of neoplastic large, polygonal epithelial cells with large vesicular nuclei and prominent nucleoli.Thymus AdenocarcinomaA thymic carcinoma that arises from epithelial cells of glandular origin.Thymus Adenosquamous CarcinomaA thymic carcinoma that arises from squamous cells and gland-like cells.Thymus CancerA rare cancer of the thymus gland.Thymus LipomaAn immune system organ benign neoplasm that is in the thymus and arises from fat cells.Thymus LymphomaA thymus cancer that arises from the thymus.Thymus Mucoepidermoid CarcinomaA mucoepidermoid carcinoma in the thymus.Thymus Squamous Cell CarcinomaA squamous cell carcinoma that is in the thymus.Thyroid AdenomaAn endocrine organ benign neoplasm that is in the thyroid and arises from glandular epithelial cells.Thyroid AngiosarcomaA thyroid sarcoma and angiosarcoma that causes a high prevalence of iodine-deficient goiter.Thyroid CancerCancer of the thyroid gland. Tracking your symptoms and connecting with others who understand can help you manage day to day.Thyroid Dyshormonogenesis 1A familial thyroid dyshormonogenesis that is caused by homozygous or compound heterozygous mutation in SLC5A5 on chromosome 19p13.11.Thyroid Dyshormonogenesis 2AA familial thyroid dyshormonogenesis that is caused by homozygous or compound heterozygous mutation in TPO on chromosome 2p25.3.Thyroid Dyshormonogenesis 3A familial thyroid dyshormonogenesis that is caused by homozygous or compound heterozygous mutation in TG on chromosome 8q24.22.Thyroid Dyshormonogenesis 4A familial thyroid dyshormonogenesis that is caused by homozygous or compound heterozygous mutation in IYD on chromosome 6q25.1.Thyroid Dyshormonogenesis 5A familial thyroid dyshormonogenesis that is caused by homozygous or compound heterozygous mutation in DUOXA2 on chromosome 15q21.1.Thyroid Dyshormonogenesis 6A familial thyroid dyshormonogenesis that is caused by homozygous or compound heterozygous mutation in DUOX2 on chromosome 15q21.1.Thyroid Eye DiseaseEye bulging and inflammation linked to thyroid problems.Thyroid Gland AdenocarcinomaA thyroid gland carcinoma that arises from epithelial cells of glandular origin.Thyroid Gland CarcinomaA thyroid gland cancer that is caused by epithelial cells.Thyroid Gland Cribriform Morular CarcinomaA thyroid gland carcinoma that is characterized by the presence of cribriform, trabecular, follicular, papillary, and solid growth patterns and squamoid morulae formation.Thyroid Gland DiseaseAn endocrine system disease that is in the thyroid.Thyroid Gland Mixed Medullary and Follicular Cell-Derived CarcinomaA thyroid gland carcinoma containing a medullary carcinoma component that is immunohistochemically positive for calcitonin, and follicular cell-derived carcinoma component that is immunohistochemically positive for thyroThyroid Gland Mucinous CarcinomaA thyroid gland carcinoma that is characterized by the presence of clusters of malignant epithelial cells associated with abundant extracellular mucin deposition.Thyroid Gland Mucoepidermoid CarcinomaA thyroid gland carcinoma that is composed of groups of squamoid and mucous cells, surrounded by fibrous tissue.Thyroid Gland Spindle Epithelial Tumor with Thymus-Like ElementsA thyroid gland carcinoma that is characterized by a lobulated architectural pattern and the presence of a biphasic cellular population composed of spindle epithelial cells and glandular cells.Thyroid LymphomaA thyroid gland cancer that is caused by lymphocytes.Thyroid NodulesLumps in the thyroid gland, usually noncancerous.Thyroid SarcomaA thyroid gland cancer that is in the supporting cells of the thyroid.ThyrotoxicosisA thyroid gland disease that is characterized by excess thyroid hormone.Tibial AdamantinomaAn adamantinoma of long bone that is in the tibia.Tibial Muscular DystrophyA distal myopathy that is characterized by autosomal dominant inheritance of late-onset muscular dystrophy beginning in the anterior compartment of the legs that is caused by heterozygous mutation in the gene encoding thTic DisorderA specific developmental disorder that is characterized by the persistent presence of involuntary brief movements or sounds occurring intermittently and unpredictably out of a background of normal motor activity.Tick-Borne EncephalitisA viral infectious disease that causes inflammation in brain, is caused by Tick-borne encephalitis virus (Orthoflavivirus encephalitidis), which is transmitted by Ixodes ticks. The infection causes drowsiness, causes conTick-Borne Relapsing FeverA relapsing fever that is characterized by relapsing or recurring episodes of fever, is caused by Borrelia hermsii, is caused by Borrelia parkeri or is caused by Borrelia duttoni, which are transmitted by soft ticks (OrnTick InfestationA parasitic ectoparasitic infectious disease that involves parasitic infestation of blood feeding ticks of the families Ixodidae and Argasidae on animals and humans. Ticks are vectors of a number diseases, including LymeTick ParalysisA tick infestation that is characterized by an acute, ascending, flaccid motor paralysis, which is caused by the introduction of a neurotoxin into humans during attachment and feeding by the females of several tick speciTietze'S SyndromeA cartilage disease that is characterized by localized tenderness and non-suppurative swelling, typically associated with the 2nd or 3rd costal cartilages unilaterally caused by inflammation of one or more of the costalTietz SyndromeA syndrome that is characterized by congenital profound bilateral sensorineural hearing loss and generalized albino-like hypopigmentation of skin, eyes and hair that is caused by mutation in the MITF gene on chromosome 3Tiger Prawn AllergyA crustacean allergy triggered by Penaeus monodon.Time AgnosiaAn agnosia that is a loss of the ability to comprehend the succession and duration of events.Timothy Grass AllergyA pollen allergy triggered by Phleum pratense pollen.Timothy SyndromeA syndrome characterized by cardiac, hand/foot, facial, and neurodevelopmental features that is caused by heterozygous mutation in the CACNA1C gene on chromosome 12p13.33. The two forms are type 1 (classic) and type 2, aTinea BarbaeA dermatophytosis that causes fungal infection which effects horny layer of epidermis of the bearded areas in face or in neck, is caused by Trichophyton mentagrophytes or is caused by Trichophyton verrucosum, which alsoTinea CapitisA dermatophytosis that causes contagious fungal infection in scalp, in hair of head, in eyebrow or in eyelash, is caused by Ascomycota fungi that belong to a group called dermatophytes and causes itching of the scalp, caTinea CorporisA dermatophytosis that causes fungal infection in skin, limited to the stratum corneum of the epidermis, is caused by Ascomycota fungi that belong to a group called dermatophytes and causes itching, and causes red coloreTinea CrurisA dermatophytosis that causes fungal skin infection in groin, in perineum, or in perianal region, is caused by Ascomycota fungi that belong to a group called dermatophytes and causes itching in groin, thigh skin folds, oTinea FavosaA tinea capitis that causes fungal infection in scalp, in glabrous skin or in nail, is caused by Ascomycota fungi that belong to a group called dermatophytes and causes the formation of scutula, yellowish cup-shaped crusTinea ImbricataA tinea corporis that causes fungal infection in skin, is caused by Trichophyton concentricum, which is characterized by ring-like growth in overlapping circles that may have an autosomal dominant genetic predisposition.Tinea ManuumA dermatophytosis that causes fungal skin infection in hand, is caused by Ascomycota fungi that belong to a group called dermatophytes and causes itching, causes burning, causes cracking, and causes scaling.Tinea NigraA superficial mycosis that is a superficial fungal infection of the skin characterized by brown to black macules which usually occur on the palmar aspects of hands and occasionally the plantar and other surfaces of the sTinea PedisA dermatophytosis that causes fungal infection in skin of foot, especially between the toes, is caused by Trichophyton or is caused by Epidermophyton and causes fissures, causes scaling, causes maceration, and eroded areTinea ProfundaA tinea corporis that causes fungal infection in skin, is caused by Trichophyton mentagrophytes and causes the formation of subcutaneous abscesses.Tinea UnguiumA dermatophytosis that causes fungal infection in nail, is caused by Ascomycota fungi that belong to a group called dermatophytes, which cause separation of the nail plate from the nail bed and causes thickening of subunTinnitusRinging or buzzing in the ears. Tracking your symptoms and connecting with others who understand can help you manage day to day.TNF Receptor–associated Periodic SyndromeAn autoinflammatory disease characterized by recurrent fever, abdominal pain, localized tender skin lesions, arthralgia and myalgia associated with skin, joint, ocular and serosal inflammation that is caused by heterozygTn Polyagglutination SyndromeA hematopoietic system disease that is characterized by red blood cells that agglutinate upon exposure to almost all human sera, but not to autologous serum or the sera of newborns and is caused by somatic mutation in thToluene 2,4-Diisocyanate Allergic AsthmaA toluene meta-diisocyanate allergic asthma that triggered by toluene 2,4-diisocyanate.Toluene Meta-Diisocyanate Allergic AsthmaAn isocyanates allergic asthma that triggered by toluene meta-diisocyanate.Tomato AllergyA fruit allergy triggered by Solanum lycopersicum plant fruit food product.Tongue CarcinomaA tongue cancer that arises from epithelial cells that cover the surface of the tongue.Tongue DiseaseA mouth disease in the tongue.Tongue Squamous Cell CarcinomaA head and neck squamous cell carcinoma that is in the tongue.Tonne-Kalscheuer SyndromeA syndromic X-linked intellectual disability characterized by global developmental delay, impaired intellectual development, speech delay, and behavioral abnormalities in most patients and variable congenital anomalies iTonsillitisInflammation of the tonsils.Tonsil Squamous Cell CarcinomaA tonsil cancer that is caused by squamous cells.Tooth AgenesisA tooth disease characterized by failure to develop one or more missing teeth.Tooth and Nail SyndromeA syndrome that affects the teeth, nails, hair, and/or skin. It is characterized by absence (hypodontia) and/or malformation of certain primary (deciduous) and secondary (permanent) teeth occurring in association with imTooth DiseaseA mouth disease in the teeth.Topographical AgnosiaAn agnosia that is a loss of the ability to rely on visual cues to guide them directionally due to the inability to recognise objects.TORCH SyndromeA syndrome that is characterized by congenital infection with toxoplasmosis, rubella, cytomegalovirus, herpes simplex, and other organisms.Torrance Type Platyspondylic DysplasiaAn osteochondrodysplasia characterized by decreased ossification of the skull base, disc-like platyspondyly, short thin ribs, hypoplastic pelvis with wide sacrosciatic notches and flat acetabular roof, and short tubularTorsion Dystonia 1A generalized dystomia characterized by autosomal dominant inheritance of dystonia usually presenting initially as focal, typically in the limbs, but often generalizes with age that is caused by heterozygous mutation inTorsion Dystonia 13A dystonia that is characterized by focal or segmental dystonia with cranial, cervical, or upper limb involvement that is caused by autosomal dominant inheritance of variation in the chromosome region 1p36.32-p36.13.Torsion Dystonia 17A dystonia that is characterized by progressive dystonia, dysphonia, dysarthria and neck torticollis, and is caused by autosomal recessive inheritance of variation in the chromosome region 20p11.2-q13.12.Torsion Dystonia 2A dystonia that initially involves the distal limbs and later involves the neck, orofacial, and craniocervical regions, and is caused by autosomal recessive inheritance of homozygous or compound heterozygous mutation inTorsion Dystonia 4A dystonia that is characterized by progressive laryngeal and cervical dystonia (onset in the second to third decade of life) followed by involvement of other muscles, such as the neck or limbs that is caused by autosomaTorsion Dystonia 6A generalized dystonia that is characterized by early-onset generalised dystonia typically involing the craniocervical region with spasmodic dysphonia that is caused by autosomal dominant inheritance of heterozygous mutaTorsion Dystonia 7A focal dystonia that is characterized by predominantly cervical dystonia that is caused by autosomal dominant inheritance of variation in the chromosome region 18p.Torsion Dystonia with Onset in InfancyA generalized dystonia that is characterized by autosomal dominant inheritance of generalized dystonia with severe involvement of the legs, mild involvement of the face and arms, and onset in infancy.Tourette SyndromeA condition with involuntary movements and sounds called tics. Tracking your symptoms and connecting with others who understand can help you manage day to day.Townes-Brocks SyndromeA syndrome that is characterized by imperforate anus, dysplastic ears often associated with sensorineural and/or conductive hearing impairment, and thumb malformations.ToxascariasisA parasitic helminthiasis infectious disease that involves parasitic infection of dogs, cats and foxes with Toxascaris leonina causing damage to the lining of the intestine. The symptoms include diarrhea, vomiting and loToxic EncephalopathyA nervous system disease that results from exposure to neurotoxicants and is characterized by an altered mental status, memory loss, and visual problems.Toxic LabyrinthitisA labyrinthitis induced by alcohol, drug ingestion, or occasionally, inhaled substances that are toxic to the inner ear. Drugs like aminoglycosides, furosemide, ethacrynic acid, acetylsalicyclic acid, amiodarone, quinineToxic MyocarditisAn acute myocarditis that is characterized by an underlying toxin insult to the myocardium that induces acute inflammation.Toxicodendron DermatitisAn allergic contact dermatitis that triggered by members of the toxicodendron family, including urushiol producing poison ivy, poison oak, and poison sumac, causes pruritic erythematous rash with papules, vesicles, and pToxic PneumonitisA pneumonia that is an acute inflammation of the lungs induced by inhalation of metal fumes or toxic gases and vapors. It is a sentinel health event (occupational) associated with exposure to ammonia (refrigeration, fertToxic Shock SyndromeA commensal bacterial infectious disease that causes infection, is caused by Streptococcus pyogenes or is caused by Staphylococcus aureus, which produce toxins that are absorbed systemically and produce the systemic maniToxocariasisA parasitic helminthiasis infectious disease that involves zoonotic infection of humans by the larvae of Toxocara canis or Toxocara cati. The larvae invade multiple tissues like liver, heart, lungs, brain, muscle and eyeToxoplasmosisA parasitic infection that can harm unborn babies.Trachea CarcinomaA tracheal cancer that effects the airway that leads from the larynx to the bronchi.Trachea Carcinoma in SituAn in situ carcinoma that is in the trachea.Tracheal CancerA respiratory system cancer that is in the trachea.Trachea LeiomyomaA respiratory system benign neoplasm that arises from smooth muscle cells and is in the trachea.Trachea Mucoepidermoid CarcinomaA mucoepidermoid carcinoma in the trachea.Trachea SarcomaA sarcoma and malignant tumor of trachea that is in the trachea.Trachea Squamous Cell CarcinomaA squamous cell carcinoma that is in the trachea.TracheitisA tracheal disease which involves bacterial infection of the trachea often caused by Staphylococcus aureus and streptococci that follows a recent viral upper respiratory infection. The symptoms include barking croup cougTracheomalaciaA tracheal disease characterized by flaccidity of the tracheal support cartilage.TrachomaA commensal bacterial infectious disease that causes infection in eye, is caused by Chlamydia trachomatis (A, B, Ba and C serovars), which is transmitted by contact with eye discharge from the infected person and transmiTranscobalamin II DeficiencyA vitamin B12 deficiency that is characterized by a lack of vitamin B12 intestinal absorption resulting from a deficiency in the B12 transport protein TCII.Transient Bullous Dermolysis of the NewbornAn epidermolysis bullosa dystrophica characterized by generalized blistering at birth that usually regresses by 6 to 24 months of age that is caused by heterozygous, compound heterozygous or homozygous mutation in COL7A1Transient Cerebral IschemiaA brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.Transient Global AmnesiaA sudden, temporary episode of memory loss.Transient Hypogammaglobulinemia of InfancyAn immune system disease characterized by a transitory drop in the levels of immunoglobulin G in an infant beginning between 5 and 24 months of age with levels typically returning to reference range by 6 years of age.Transient Infantile Liver FailureA liver disease that is characterized by elevated liver enzymes, jaundice, vomiting, coagulopathy, and hyperbilirubinemia, and the presence of increased serum lactate and that is caused by homozygous or compound heterozyTransient Ischemic AttackA temporary stroke-like episode that resolves within minutes.Transient Myeloproliferative SyndromeA myeloproliferative neoplasm characterized by leukocytosis in newborns with Down syndrome.Transient Neonatal Diabetes MellitusA neonatal diabetes that is characterized by hyperglycemia during the neonatal period that remits during infancy but recurs in later life in most patients.Transient Neonatal Diabetes Mellitus 1A transient neonatal diabetes mellitus that is caused by overexpression of the paternal allele of the imprinted locus at chromosome 6q24, which contains only 2 expressed genes, PLAGL1 and HYMAI.Transient Neonatal Diabetes Mellitus 2A transient neonatal diabetes mellitus that is caused by heterozygous mutation in the ABCC8 gene on chromosome 11p15.Transient Neonatal Diabetes Mellitus 3A transient neonatal diabetes mellitus that is caused by heterozygous mutation in the KCNJ11 gene on chromosome 11p15.Transient Tic DisorderA tic disorder that consists of multiple motor and/or phonic tics with duration of at least 4 weeks, but less than 12 months.Transitional Cell CarcinomaA carcinoma that arises from transitional epithelial cells.Transverse MyelitisA myelitis that is characterized by a band-like sensation across the trunk of the body, with sensory changes below.TRAPS SyndromeA rare autoinflammatory disease causing recurrent fevers.Traumatic Brain InjuryBrain damage from a blow or jolt to the head.Traumatic GlaucomaA glaucoma characterized by elevated intraocular pressure secondary to ocular trauma, which leads to glaucomatous optic nerve atrophy and progressive vision loss and causes progressive decreased vision, visual field defeTreacher Collins SyndromeA syndrome that is characterized by bilateral and symmetric downslanting palpebral fissures, malar hypoplasia, micrognathia, and external ear abnormalities.Treacher Collins Syndrome 1A Treacher Collins syndrome that is caused by heterozygous mutation in the 'treacle' gene (TCOF1) on chromosome 5q32.Treacher Collins Syndrome 2A Treacher Collins syndrome that is caused by heterozygous mutation in the POLR1D gene on chromosome 13q12.Treacher Collins Syndrome 3A Treacher Collins syndrome that is caused by compound heterozygous mutation in the POLR1C gene on chromosome 6p21.Treacher Collins Syndrome 4A Treacher Collins syndrome that is characterized by craniofacial dysmorphisms including downslanting palpebral fissures, malar and mandibular hypoplasia, and microtia and that is caused by heterozygous mutation in the PTrench FeverA primary bacterial infectious disease that results in systemic infection, is caused by Bartonella quintana, which is transmitted by body lice (Pediculus humanus corporis). The infection has symptom relapsing fever, hasTrichinosisA parasitic helminthiasis infectious disease that involves parasitic infection of animals and humans by Trichinella spiralis, Trichinella nativa or Trichinella britovi. Intestinal invasion causes diarrhea, abdominal painTrichodontoosseous SyndromeA syndrome characterized by curly kinky hair at birth, enamel hypoplasia, taurodontism, thickening of cortical bones and variable expression of craniofacial morphology that is caused by heterozygous mutation in the DLX3Trichohepatoenteric SyndromeA syndrome characterized by intractable diarrhea, facial dysmorphism, immune abnormalities, and hair abnormalities in nearly all patients with liver and/or skin abnormalities seen in more than half of cases that is causeTrichohepatoenteric Syndrome 1A trichohepatoenteric syndrome that is caused by homozygous or compound heterozygous mutation in the TTC37 gene on chromosome 5q15.Trichohepatoenteric Syndrome 2A trichohepatoenteric syndrome that is caused by homozygous or compound heterozygous mutation in the SKIV2L gene on chromosome 6p21.33.Trichomonas Tenax TrichomoniasisA 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 periodonitTrichomonas Vaginalis TrichomoniasisA trichomoniasis that involves infection of the urogenital tract, is caused by Trichomonas vaginalis, which is transmitted through sexual contact. Symptoms include inflammation of the cervix, urethra and vagina which proTrichomoniasisA parasitic sexually transmitted infection.Trichorhinophalangeal Syndrome Type IA syndrome that is characterized by short stature, sparse hair, a bulbous nasal tip and cone-shaped epiphyses (the growing ends of bones), as well as severe generalized shortening of all finger and toe bones (brachydactyTrichorhinophalangeal Syndrome Type IIA syndrome that is caused by mutation of the EXT1 and TRPS1 gene which causes multiple exostosis along with short stature and cone-shaped ends in epiphysis. The disease causes sparse scalp hair, causes thin upper lip, caTrichorhinophalangeal Syndrome Type IIIA syndrome that is characterized by sparse hair, beaked nose, long upper lip, and severe metacarpophalangeal shortening and is caused by heterozygous mutation in the TRPS1 gene on chromosome 8q23.TrichosporonosisAn opportunistic mycosis that causes disseminated infection, is caused by Trichosporon and causes the formation of nontender erythematous nodules anywhere on the body.TrichostrongyloidiasisA parasitic helminthiasis infectious disease that involves parasitic infection of animals and humans by nematodes of the superfamily Trichostrongyloidea.TrichostrongylosisA trichostrongyloidiasis that involves infection of the small intestine with Trichostrongylus colubriformis or Trichostrongylus axei, which results in abdominal pain, diarrhea, anorexia, headache, fatigue, anemia and eosTrichothiodystrophyA syndrome characterized by sparse, brittle, sulfur-deficient hair that is easily broken and in more severe cases delayed development, significant intellectual disability, and recurrent infections.TrichotillomaniaCompulsive hair pulling.TrichuriasisA parasitic helminthiasis infectious disease that involves parasitic infection in intestine in humans, is caused by Trichuris trichiura, which is transmitted by ingestion of food contaminated with egg-carrying soil. TheTricuspid AtresiaA tricuspid valve disease characterized by a missing or abnormally developed tricuspid heart value at birth.Tricuspid Valve DiseaseA heart valve disease that is characterized by valvular insufficiency or valvular stenosis, in tricuspid valve between the right atrium and right ventricle.Tricuspid Valve InsufficiencyA tricuspid valve disease that is characterized by failure of the heart's tricuspid valve to close properly during systole. As a result, with each heart beat, blood is pumped out from the right side of the heart in the oTricuspid Valve StenosisA tricuspid valve disease that is characterized by the narrowing of the orifice of the tricuspid valve of the heart. This causes increased resistance to blood flow through the valve.Trigeminal NeuralgiaSudden, severe facial pain from the trigeminal nerve. Tracking your symptoms and connecting with others who understand can help you manage day to day.Trigger FingerA finger that locks or catches when bent.Trilateral RetinoblastomaA retinoblastoma that refers to bilateral retinoblastoma associated with an intracranial primitive neuroectodermal tumor in the pineal or suprasellar region.Trimellitic Anhydride Allergic AsthmaAn allergic asthma that triggered by trimellitic anhydride.Trimethoprim AllergyA drug allergy that triggered by trimethoprim.TrimethylaminuriaAn inherited metabolic disorder characterized by the inability to break down trimethylamine and is caused by homozygous or compound heterozygous mutation in the gene encoding flavin-containing monooxygenase-3 on chromosoTriosephosphate Isomerase DeficiencyA glucose metabolism disorder that is characterized by chronic haemolytic anaemia, cardiomyopathy, susceptibility to infections and severe neurological dysfunction, and is caused by the triosephosphate isomerase enzyme (Triple-a SyndromeA syndrome characterized by achalasia, adrenal insufficiency and alacrima and is caused by mutations in the AAAS gene that encodes ALADIN within the nuclear envelope and results in dysfunction of the autonomic nervous syTriple-Negative Breast CancerA breast cancer that is characterized by the absence of estrogen, progresterone and HER2 (EBBR2) receptors.Triple Positive Breast CancerA hormone receptor-positive/HER2-positive breast cancer characterized by excess HER2 (ERBB2) protein and the presence of both estrogen and progesterone receptors.TrombiculiasisA mite infestation that involves rash caused by Leptotrombidium deliense.Trophoblastic NeoplasmA germ cell and embryonal cancer that arises from trophoblastic tissue.Troyer SyndromeA 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 delaTrypanosomiasisA parasitic protozoa infectious disease that involves infection caused by parasitic protozoan of the genus Trypanosoma in animals and humans.Tuberculoid LeprosyA leprosy that results in one erythematous large plaque with well-defined borders that are elevated and that slope down into an atrophic center.TuberculosisA bacterial infection that mainly affects the lungs.Tuberculous EmpyemaA pleural empyema which involves presence of pus in the pleural cavity and calcified visceral pleura. It results from a large number of mycobacteria spilling into the pleural space, usually from rupture of a cavity or anTuberculous EncephalopathyA tuberculosis that is characterized by cerebral edema sometimes with features similar to acute disseminated encephalomyelitis (ADEM) and may manifest with a variety of symptoms ranging from focal neurological deficits tTuberculous EpididymitisAn urogenital tuberculosis that is in epididymis, causes pain and causes scrotal swelling.Tuberculous OophoritisAn urogenital tuberculosis that causes inflammtion in ovary.Tuberculous PeritonitisA gastrointestinal tuberculosis that causes inflammation in peritoneum, which results in formation of tubercles. The infection causes abdominal discomfort, causes pain, causes distention from gas or fluid, causes digestiTuberculous PneumothoraxA pneumothorax in which air enters into the pleural cavity.Tuberculous SalpingitisAn urogenital tuberculosis that causes formation of granulomas in fallopian tube.Tuberous SclerosisA genetic disorder causing noncancerous tumors in organs.Tuberous Sclerosis 1A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and is caused by heterozygous mutation in the TSC1 gene on chromosome 9q34.Tuberous Sclerosis 2A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and is caused by autosomal dominant inheritance of heterozygous mutation in the TSC2 gene, which encodes tuberin, on chromosome 16p13.Tubocurarine AllergyA drug allergy that triggered by tubocurarine.Tubular AdenocarcinomaAn adenocarcinoma that arises from epithelial cells originating in glandular tissue. The tumor has branched angular tubules embedded in a loose fibrous stroma.Tubular Aggregate Myopathy 1A myopathy that is characterized by the presence of tubular aggregates in myofibrils and is caused by heterozygous mutation in the STIM1 gene on chromosome 11p15.Tubular Aggregate Myopathy 2A myopathy that is characterized by the presence of tubular aggregates in myofibrils and is caused by heterozygous mutation in the ORAI1 gene on chromosome 12q24.TubulinopathyA congenital nervous system abnormality characterized by complex cortical malformations including in most cases dysmorphic basal ganglia that is caused by mutation in one or more of the tubulin genes.Tukel SyndromeA congenital fibrosis of the extraocular muscles that is characterized by nonprogressive restrictive ophthalmoplegia with blepharoptosis of the right eye and postaxial oligodactyly/oligosyndactyly of the hands, with theTularemiaA primary bacterial infectious disease that is caused by Francisella tularensis, which is transmitted by dog tick bite (Dermacentor variabilis), transmitted by deer flies (Chrysops sp) or transmitted by contact with infeTungiasisA 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 inflammatiTurner SyndromeA condition from a missing or incomplete X chromosome.Twin-to-Twin Transfusion SyndromeA neonatal anemia that is characterized by an increased number of arteriovenous anastomoses deep in the placenta. These capillary connections occur in the cotyledon portion of the placenta. Unidirectional flow can occurType 1 DiabetesAn autoimmune condition where the pancreas stops making insulin.Type 1 Diabetes MellitusA diabetes mellitus that is characterized by destruction of pancreatic beta cells resulting in absent or extremely low insulin production.Type 1 Diabetes Mellitus 10A type 1 diabetes mellitus that is caused by mutation of the IL2RA gene on chromosome 10p15.1.Type 1 Diabetes Mellitus 11A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 14q24.3-q31.Type 1 Diabetes Mellitus 12A type 1 diabetes mellitus that is caused by mutation of the CTLA4 gene on chromosome 2q33.2.Type 1 Diabetes Mellitus 13A type 1 diabetes mellituss that is caused by mutation of the locus at chromosome 2q34.Type 1 Diabetes Mellitus 15A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 6q21.Type 1 Diabetes Mellitus 17A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 10q25.Type 1 Diabetes Mellitus 18A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 5q31.1-q33.1.Type 1 Diabetes Mellitus 19A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 2q24.3.Type 1 Diabetes Mellitus 2A type 1 diabetes mellitus that is caused by autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5.Type 1 Diabetes Mellitus 20A type 1 diabetes mellitus that is caused by mutation of the HNF1A gene on chromosome 12q24.31.Type 1 Diabetes Mellitus 21A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 6q25.Type 1 Diabetes Mellitus 22A type 1 diabetes mellitus that is caused by mutation of the CCR5 gene on chromosome 3p21.31.Type 1 Diabetes Mellitus 23A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 4q27.Type 1 Diabetes Mellitus 24A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 10q23.31.Type 1 Diabetes Mellitus 3A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 15q26.Type 1 Diabetes Mellitus 4A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 11q13.Type 1 Diabetes Mellitus 5A type 1 diabetes mellitus that is caused by mutation of the SUMO4 gene on chromosome 6q25.1.Type 1 Diabetes Mellitus 6A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 18q21.Type 1 Diabetes Mellitus 7A type 1 diabetes mellitus that is caused by mutation of the locus at chromosome 2q31.Type 1 Diabetes Mellitus 8A type 1 diabetes mellituss that is caused by mutation of the locus at chromosome 6q25-q27.Type 2 DiabetesThe body becomes resistant to insulin or doesn't make enough.Type 2 Diabetes MellitusA diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.Type I Complement Component 8 DeficiencyA complement deficiency that is characterized by deficiency of the alpha subunit of complement protein 8, which causes increased susceptibility to recurrent bacterial infections, especially to Neisseria meningitidis, andType II Complement Component 8 DeficiencyA complement deficiency that is characterized by deficiency of the beta subunit of complement protein 8, which causes increased susceptibility to recurrent bacterial infections, especially to Neisseria meningitidis, andTyphoidal TularemiaA tularemia that causes bacteremia and causes fever, causes chills, causes myalgia, causes malaise, and causes weight loss.Typhoid FeverA bacterial infection from contaminated food or water.TyphusA primary bacterial infectious disease that refers to a group of diseases, located in endothelial cells of the small venous, arterial, and capillary vessels, is caused by Rickettsia bacteria, which are transmitted by licTypical Adult-Onset Autosomal Dominant Demyelinating LeukodystrophyAn adult onset demyelinating leukodystrophy characterized by autonomic abnormalities, pyramidal and cerebellar dysfunction, and symmetric demyelination of the CNS, presenting in the fourth or fifth decade of life, and thTyrosinemiaAn amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine.Tyrosinemia Type IA tyrosinemia that is caused by deficiency of the enzyme fumarylacetoacetate hydrolase resulting in an increase in fumarylacetoacetate which inhibits previous steps in tyrosine degradation leading to an accumulation of tTyrosinemia Type IIA tyrosinemia that is caused by deficiency of hepatic tyrosine aminotransferase in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels.Tyrosinemia Type IIIA tyrosinemia that is caused by deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine.
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