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Disease	Synonyms	Description	Articles
intestinal tuberculosis	tuberculosis of intestine	A gastrointestinal tuberculosis that involves diff..[+] A gastrointestinal tuberculosis that involves diffuse mucosal fold thickening, formation of ulcers and fistulae located_in intestine. The infection has_symptom abdominal pain, has_symptom gastrointestinal bleeding, has_symptom nausea and has_symptom vomiting. [-]
hypertrophy of tongue papillae	Tongue papillary hypertrophy; Tongue papillary hyp.. [+] Tongue papillary hypertrophy; Tongue papillary hypertrophy NOS (disorder); hypertrophy of tongue papillae (disorder) [-]	n_a
congenital toxoplasmosis	Toxoplasmosis - congen.; Congenital toxoplasmosis; .. [+] Toxoplasmosis - congen.; Congenital toxoplasmosis; Congenital toxoplasmosis (disorder) [-]	A toxoplasmosis that involves a reactivated infect..[+] A toxoplasmosis that involves a reactivated infection of the mother transmitted to the fetus during pregnancy. Spontaneous abortion and stillbirth may occur. [-]
scrub typhus	Typhus fever due to Rickettsia tsutsugamushi; Tsut.. [+] Typhus fever due to Rickettsia tsutsugamushi; Tsutsugamushi disease; Tsutsugamushi; Tropical typhus; Tsutsugamushi fever; Chigger-borne rickettsiosis; Japanese river fever; Chigger-borne typhus; Kedani fever; Mite-borne rickettsiosis; Mite-borne typhus; Scrub (mite-borne) typhus; Scrub mite-borne typhus [-]	A typhus that has_material_basis_in Orientia tsuts..[+] A typhus that has_material_basis_in Orientia tsutsugamushi, which is transmitted by trombiculid mites (Leptotrombidium deliense). The infection has symptom fever, has symptom headache, has symptom muscle pain, has symptom cough, has symptom maculopapular rash, has symptom eschar, has symptom splenomegaly and has symptom lymphadenopathy. [-]
acquired tear duct stenosis	Tear duct - acquired stenosis; acquired stenosis o.. [+] Tear duct - acquired stenosis; acquired stenosis of nasolacrimal duct; acquired nasolacrimal duct stenosis; Stenosis of nasolacrimal duct, acquired [-]	n_a
anodontia	Total anodontia of permanent and deciduous teeth; .. [+] Total anodontia of permanent and deciduous teeth; Complete absence of teeth; Developmental absence of tooth [-]	A tooth disease that is characterized by complete ..[+] A tooth disease that is characterized by complete absence of permanent teeth. [-]
mature cataract	Total or mature cataract; Total, mature senile cat.. [+] Total or mature cataract; Total, mature senile cataract [-]	A senile cataract that is characterized by full wh..[+] A senile cataract that is characterized by full white or brunescent opacification of the lens of the eye such that the red reflex is obscured. It is a later stage of senile cataracts and is caused by a multifactorial etiology related to aging. [-]
familial combined hyperlipidemia	type IIb hyperlipoproteinemia; familial combined h.. [+] type IIb hyperlipoproteinemia; familial combined hyperlipidemia (disorder); familial combined hyperlipidemia (disorder) [Ambiguous]; familial multiple lipoprotein-type hyperlipidemia (disorder); mixed hyperlipidemia; mixed hyperlipidemia (disorder); mixed hyperlipidaemia; hyperbetalipoproteinemia with prebetalipoproteinemia; familial multiple lipoprotein-type hyperlipidemia [-]	n_a
familial hypercholesterolemia	type II hyperlipidemia; familial hypercholesteremi.. [+] type II hyperlipidemia; familial hypercholesteremia; Fredrickson type IIa hyperlipoproteinemia; familial hyperbetalipoproteinaemia; Fredrickson type IIa lipidaemia; hyperbetalipoproteinemia [-]	A familial hyperlipidemia characterized by very hi..[+] A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. [-]	1 articles
white piedra	Tinea blanca; White piedra (disorder); White piedr.. [+] Tinea blanca; White piedra (disorder); White piedra [-]	A superficial mycosis that is a superficial fungal..[+] A superficial mycosis that is a superficial fungal infection of the hair shaft caused by Trichosporon beigelii. Infected hairs develop soft greyish-white nodules along the shaft. [-]
necrotizing ulcerative gingivitis	Trench mouth; trench mouth; (Vincent's angina) or .. [+] trench mouth; Trench mouth; (Vincent's angina) or (trench mouth); acute necrotising ulcerative gingivostomatitis [Ambiguous]; acute necrotizing ulcerative gingivostomatitis (disorder); Vincent's Angina; Vincent's angina - pharyngitis (disorder); acute necrotising ulcerative gingivitis [Ambiguous]; Vincent's angina NOS; acute necrotizing ulcerative gingivostomatitis; Angina - Vincents; acute necrotising ulcerative gingivitis; acute necrotising ulcerative gingivostomatitis; acute necrotizing ulcerative gingivitis; acute ulceromembranous gingivitis; ANUG; early acute necrotising gingivitis; Vincent angina; Vincent's angina; Vincent's angina - pharyngitis; Vincent's disease; Vincent's infection, any site [-]	n_a
epicondylitis	tennis elbow; Lateral epicondylitis; andrel epicon.. [+] tennis elbow; Lateral epicondylitis; andrel epicondylitis; archer's elbow; golfer's elbow; hockey elbow; medial epicondylitis; shooter's elbow [-]	A bone inflammation disease that results_in inflam..[+] A bone inflammation disease that results_in inflammation located_in epicondyle. [-]
De Quervain disease	Tenosynovitis, de Quervain's; Radial styloid tenos.. [+] Tenosynovitis, de Quervain's; Radial styloid tenosynovitis [-]	n_a
dihydropyrimidine dehydrogenase deficiency	thymine-uracilurea; thymine-uracilurea; Dihydropyr.. [+] thymine-uracilurea; thymine-uracilurea; Dihydropyrimidine dehydrogenase deficiency (disorder); Dihydropyrimidine dehydrogenase deficiency; Dihydrouracil Dehydrogenase deficiency; familial pyrimidinaemia [-]	A purine-pyrimidine metabolic disorder that is an ..[+] A purine-pyrimidine metabolic disorder that is an autosomal recessive metabolic disorder in which there is absent or significantly decreased activity of dihydropyrimidine dehydrogenase, an enzyme involved in the metabolism of uracil and thymine. [-]
Down syndrome	trisomy 21 syndrome; Complete trisomy 21 syndrome .. [+] trisomy 21 syndrome; Complete trisomy 21 syndrome (disorder); Down's syndrome; G Trisomy; Downs syndrome; Down's syndrome - trisomy 21; Complete trisomy 21 syndrome [-]	A chromosomal disease that is characterized by fla..[+] A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. [-]	7 articles
oral candidiasis	thrush; Thrush, oral; Candidiasis of mouth; Oral m.. [+] Thrush, oral; thrush; Candidiasis of mouth; Oral moniliasis [-]	A candidiasis that involves fungal infection of th..[+] A candidiasis that involves fungal infection of the mucous membrane of the mouth by Candida species, which is characterized by thick white or cream-colored deposits on inflamed mucosal membranes. [-]
parietal lobe neoplasm	tumor of Parietal Lobe; malignant neoplasm of pari.. [+] tumor of Parietal Lobe; malignant neoplasm of parietal lobe [-]	A cerebrum cancer that is located_in the parietal ..[+] A cerebrum cancer that is located_in the parietal lobe. [-]
Niemann-Pick disease	Type A Niemann-Pick Disease; lipoid histiocytosis .. [+] Type A Niemann-Pick Disease; lipoid histiocytosis (classical phosphatide); Niemann-Pick disease type A; Niemann-Pick disease type B; Niemann-Pick disease type C; Niemann-Pick disease with cholesterol esterification block; Niemann-Pick disease, subacute juvenile form; sphingomyelin lipidosis; Sphingomyelinase Deficiency Disease; lipoid histiocytosis [-]	A sphingoliidosis characterized by the accumulatio..[+] A sphingoliidosis characterized by the accumulation of the lipid sphingomyelin in lysosomes in cells. [-]
Ehlers-Danlos syndrome classic type 1	type I Ehlers-Danlos syndrome; Ehlers-Danlos syndr.. [+] type I Ehlers-Danlos syndrome; Ehlers-Danlos syndrome, type 1 (disorder); Ehlers-Danlos syndrome, type 1 [-]	An Ehlers-Danlos syndrome that is characterized by..[+] An Ehlers-Danlos syndrome that is characterized by loose-jointedness and fragile, bruisable skin that heals with peculiar 'cigarette-paper' scars and that has_material_basis_in heterozygous mutation in the collagen alpha-1(V) gene (COL5A1) on chromosome 9q34. [-]
Ehlers-Danlos syndrome hypermobility type	type III Ehlers-Danlos syndrome; Ehlers-Danlos syn.. [+] type III Ehlers-Danlos syndrome; Ehlers-Danlos syndrome, type 3 (disorder); Ehlers-Danlos syndrome, type 3 [-]	An Ehlers-Danlos syndrome that is characterized by..[+] An Ehlers-Danlos syndrome that is characterized by joint hyperextensibility without skeletal deformity. [-]
brittle cornea syndrome 1	type VIB Ehlers-Danlos syndrome; brittle cornea sy.. [+] type VIB Ehlers-Danlos syndrome; brittle cornea syndrome 2; Kyphoscoliosis type [-]	An Ehlers-Danlos syndrome that is characterized by..[+] An Ehlers-Danlos syndrome that is characterized by blue sclerae, corneal rupture after minor trauma, keratoconus or keratoglobus, hyperelasticity of the skin, and hypermobility of the joints and has_material_basis_in homozygous mutation in the ZNF469 gene on chromosome 16q24. [-]
olivopontocerebellar atrophy	Thomas' syndrome; Dejerine-Thomas syndrome; WADIA-.. [+] Thomas' syndrome; Dejerine-Thomas syndrome; WADIA-SWAMI SYNDROME [-]	A neurodegenerative disease that is characterized ..[+] A neurodegenerative disease that is characterized by progressive cerebellar ataxia, leading to clumsiness in body movements, veering from midline when walking, wide-based stance, and falls without signs of paralysis or weakness and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in degeneration of neuron in the cerebellum, pons and inferior olives. [-]
carbamazepine allergy	Tegretol allergy; carbamazepen allergy	A drug allergy that has_allergic_trigger carbamaze..[+] A drug allergy that has_allergic_trigger carbamazepine. [-]
ceftazidime allergy	Tazicef allergy; Fortaz allergy	A cephalosporin allergy that has_allergic_trigger ..[+] A cephalosporin allergy that has_allergic_trigger ceftazidime. [-]
co-trimoxazole allergy	trimethoprim/sulfamethoxazole allergy; TMP/SMX all.. [+] trimethoprim/sulfamethoxazole allergy; TMP/SMX allergy; Bactrim allergy; cotrimoxazol allergy [-]	A drug allergy that has_allergic_trigger co-trimox..[+] A drug allergy that has_allergic_trigger co-trimoxazole. [-]
Flinders Island spotted fever	Thai tick typhus; FISF	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. [-]
Rocky Mountain spotted fever	Tick typhus; Tick typhus; Tobia fever; Brazillian .. [+] Tobia fever; Tick typhus; Tick typhus; Brazillian spotted; Choix; Brazilian spotted; Exanthematic typhus of Sao Paulo; Fiebre maculosa; Fiebre manchada; Sao Paulo typhus; So Paulo fever [-]	A spotted fever that has_material_basis_in Rickett..[+] A spotted fever that has_material_basis_in Rickettsia rickettsii, which is transmitted_by ticks (Dermacentor variabilis and Dermacentor andersoni). The infection has_symptom fever, has_symptom headache, has_symptom abdominal pain, and has_symptom maculopapular rash progressing into papular or petechial rash. [-]
nonepidermolytic palmoplantar keratoderma	tylosis; Thost-Unna Syndrome; Unna-Thost Syndrome; .. [+] Thost-Unna Syndrome; tylosis; Unna-Thost Syndrome; NEPPK; diffuse nonepidermolytic palmomplantar keratoderma [-]	A palmoplantar keratosis characterized by a well-d..[+] A palmoplantar keratosis characterized by a well-demarcated, symmetric keratoderma located_in palms and located_in soles. [-]
Antley-Bixler syndrome with disordered steroidogenesis	trapezoidocephaly-synostosis syndrome	An Antley-Bixler syndrome that is characterized at..[+] An Antley-Bixler syndrome that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene. [-]
endemic typhus	toulon typhus; cat flea rickettsiosis; fleaborne t.. [+] toulon typhus; cat flea rickettsiosis; fleaborne typhus; murine typhus; Rat-Flea Typhus; Rickettsia felis spotted fever; Shop typhus; urban typhus; Urban Typhus of Malaya [-]	A typhus that has_material_basis_in Rickettsia typ..[+] A typhus that has_material_basis_in Rickettsia typhi or has_material_basis_in Rickettsia felis, which are transmitted by fleas (Xenopsylla cheopis). The infection has symptom headache, has symptom fever, has symptom chills, has symptom myalgia, has symptom nausea, has symptom vomiting, has symptom cough and has symptom rash. [-]
nonphotosensitive trichothiodystrophy 4	TTD4; BIDS SYNDROME; AMISH BRITTLE HAIR BRAIN SYND.. [+] TTD4; BIDS SYNDROME; AMISH BRITTLE HAIR BRAIN SYNDROME; BIDS syndrome; HAIR-BRAIN SYNDROME [-]	A nonphotosensitive trichothiodystrophy that is ch..[+] A nonphotosensitive trichothiodystrophy that is characterized by brittle hair, short stature, decreased fertility and cognitive impairment without photosensitivity has_material_basis_in mutations in the TTDN1 gene. [-]
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 a mutation in the RET gene on chromosome 10. Familial MTC can also be caused by mutations in the NTRK1 gene located on 1q21-q22. [-]
asphyxiating thoracic dystrophy	thoracic pelvic phalangeal dystrophy; Jeune syndro.. [+] thoracic pelvic phalangeal dystrophy; Jeune syndrome; short-rib thoracic dysplasia with or without polydactyly [-]	A bone development disease characterized by skelet..[+] A bone development disease characterized by skeletal abnormalities and resulting in difficulty in breathing caused by mutations that result in ciliopathy. [-]	1 articles
biliary tract benign neoplasm	tumor of the extrahepatic bile duct; neoplasm of e.. [+] tumor of the extrahepatic bile duct; neoplasm of extrahepatic bile ducts (disorder); extrahepatic bile duct neoplasm; neoplasm of extrahepatic bile ducts [-]	A hepatobiliary benign neoplasm located_in the bil..[+] A hepatobiliary benign neoplasm located_in the biliary tract. [-]
nicotine dependence	tobacco use disorder	A substance dependence that is characterized by a ..[+] A substance dependence that is characterized by a physical dependence on nicotine. [-]	1 articles
X-linked severe combined immunodeficiency	thymic epithelial hypoplasia; SCID-X1; XSCID; X-Li.. [+] thymic epithelial hypoplasia; SCID-X1; XSCID; X-Linked Severe Combined Immunodeficiency; gamma chain deficiency [-]	A severe combined immunodeficiency that is a X-lin..[+] A severe combined immunodeficiency that is a X-linked SCID that has_material_basis_in mutations in genes encoding common gamma chain proteins shared by the interleukin (IL-2,4,7,9,16 and21) receptors resulting in a non-functional gamma chain, defective interleukin signalling, minimal or ascent T- and NK cells and non-functional B-cells. [-]
immunodeficiency with hyper IgM type 3	type 3 hyper-IgM immunodeficiency; type 3 hyper-Ig.. [+] type 3 hyper-IgM immunodeficiency; type 3 hyper-IgM immunodeficiency; immunodeficiency with hyper-IgM type 3; hyper-IgM syndrome due to CD40 deficiency; HIGM3; CD40 deficiency [-]	A hyper IgM syndrome that has_material_basis_in mu..[+] A hyper IgM syndrome that has_material_basis_in mutation in the TNFRSF5 gene, resulting in type 3 hyper-IgM immunodeficiency that is characterized by an inability of B cells to undergo isotype switching, an inability to mount an antibody-specific immune response, and a lack of germinal center formation. [-]
Good syndrome	thymoma with hypogammaglobulinemia	A combined T cell and B cell immunodeficiency that..[+] A combined T cell and B cell immunodeficiency that is a condition where there is co-occurrence of deficient cell-mediated immunity and benign thymoma. [-]
connective tissue benign neoplasm	tumor of the soft tissue; soft tissue benign neopl.. [+] tumor of the soft tissue; soft tissue benign neoplasm; neoplasm of soft tissue; neoplasm of soft tissues; mesenchymal tissue neoplasm [-]	A musculoskeletal system benign neoplasm that is l..[+] A musculoskeletal system benign neoplasm that is located_in connective tissue. [-]
amyotrophic lateral sclerosis type 10	TARDBP-related frontotemporal lobar degeneration w.. [+] TARDBP-related frontotemporal lobar degeneration with TDP43 inclusions; ALS10; amyotrophic lateral sclerosis 10; amyotrophic lateral sclerosis 10, with or without frontotemporal dementia [-]	An amyotrophic lateral sclerosis that has_material..[+] An amyotrophic lateral sclerosis that has_material_basis_in mutation in the TARDBP gene on chromosome 1. [-]
Balo concentric sclerosis	Tumefactive multiple sclerosis; Balo's concentric .. [+] Tumefactive multiple sclerosis; Balo's concentric sclerosis; Balo disease [-]	A multiple sclerosis that is characterized by conc..[+] A multiple sclerosis that is characterized by concentric layers of demyelinated tissues, tumor-like lesions larger than two centimeters and symptoms similar to those of a brain tumor. [-]
3-M syndrome	three M syndrome; Miller-McKusick-Malvaux syndrome.. [+] three M syndrome; Miller-McKusick-Malvaux syndrome; dolichospondylic dysplasia; gloomy face syndrome; Le Merrer syndrome; Yakut short stature syndrome [-]	A syndrome characterized by dwarfism, facial dysmo..[+] A syndrome characterized by dwarfism, facial dysmorphia and skeletal abnormalities. [-]
Stormorken syndrome	thrombocytopathy, asplenia and miosis	A blood platelet disease characterized by thromboc..[+] A blood platelet disease characterized by thrombocytopathy, thrombocytopenia, mild anemia, asplenia, tubular aggregate myopathy, miosis, headache, and ichthyosis. It has_material_basis_in heterozygous mutation in the STM1 gene on chromosome 11p15. It has an autosomal dominant inheritance pattern. [-]
distal 10q deletion syndrome	terminal chromosome 10q26 deletion syndrome; telom.. [+] terminal chromosome 10q26 deletion syndrome; telomeric deletion 10q; chromosome 10q26 deletion syndrome; monosomy 10qter; distal monosomy 10q [-]	A chromosomal deletion syndrome that is characteri..[+] A chromosomal deletion syndrome that is characterized by developmental delay, intellectual disability, behavioral problems and facial facies caused by a missing copy of the long arm of chromosome 10. [-]
chromosome 15q26-qter deletion syndrome	telomeric 15q deletion syndrome; 15q26 deletion sy.. [+] telomeric 15q deletion syndrome; 15q26 deletion syndrome; distal 15q deletion syndrome; distal monosomy 15q; Drayer syndrome [-]	A chromosomal deletion syndrome that is characteri..[+] A chromosomal deletion syndrome that is characterized by pre- and postnatal growth restriction, developmental delay, variable degrees of intellectual disability, brachy-clinodactyly, talipes equinovarus, nail hypoplasia, proximally placed digits and mild craniofacial dysmorphism including microcephaly, triangular face, broad nasal bridge and micrognathia. [-]	1 articles
chromosome 16p13.3 duplication syndrome	telomeric duplication 16p; distal trisomy 16p; 16p.. [+] telomeric duplication 16p; distal trisomy 16p; 16p13.3 microduplication syndrome; distal duplication 16p [-]	A chromosomal duplication syndrome that has_materi..[+] A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 16p13.3 region. [-]
chromosome 17p13.3 duplication syndrome	trisomy 17p13.3; 17p13.3 duplication syndrome; 17p.. [+] trisomy 17p13.3; 17p13.3 duplication syndrome; 17p13.3 microduplication syndrome; chromosome 17p13.3 centromeric duplication syndrome [-]	A chromosomal duplication syndrome that has_materi..[+] A chromosomal duplication syndrome that has_material_basis_in the PAFAH1B1 and/or the YWHAE gene on chromosome 17p13.3. [-]
chromosome 17q12 duplication syndrome	trisomy 17q12; 17q12 microduplication syndrome	A chromosomal duplication syndrome that has_materi..[+] A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 17q12 region. [-]
chromosome 17q21.31 duplication syndrome	trisomy 17q21.31; 17q21.31 microduplication syndro.. [+] trisomy 17q21.31; 17q21.31 microduplication syndrome [-]	A chromosomal duplication syndrome that has_materi..[+] A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 17q21.31 region. [-]
chromosome 1q21.1 duplication syndrome	trisomy 1q21.1; 1q21.1 microduplication syndrome	A chromosomal duplication syndrome that has_materi..[+] A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 1q21.1 region. [-]

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