Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
gastrointestinal tularemia	DOID_14239	[A tularemia that results in formation of ulcerative lesions located in gastrointestinal tract. The infection has symptom fever, has symptom chills, has symptom malaise, has symptom muscle aches, and has symptom vomiting.]
adrenal gland	UBERON_0002369
scleromalacia perforans	DOID_14230
tympanic membrane	UBERON_0002364
orbital cyst	DOID_14233
osteoarthritis susceptibility 1	OMIM_165720
chronic purulent otitis media	DOID_14247	[A suppurative otitis media which is persistent and long-lasting.]
chronic atticoantral disease	DOID_14248	[A chronic purulent otitis media which involves perforation in the attic region (pars flaccida of the tympanic membrane) or at the posterosuperior margin, with in-growth of squamous epithelium into the middle ear. This is caused as a result of poor ventilation of the middle ear and episodes of infection.]
Abnormality of the femoral neck or head region	HP_0003366
chronic perichondritis of pinna	DOID_14243	[A perichondritis of auricle which is persistent and long-lasting.]
epiphora due to excess lacrimation	DOID_14244
cystoid macular retinal degeneration	DOID_14245
lacrimal gland cancer	DOID_294
Pediculus	NCBITaxon_121222
pleomorphic adenoma carcinoma	DOID_297
mixed lacrimal gland cancer	DOID_296
Pediculidae	NCBITaxon_121221
eye carcinoma	DOID_295	[An ocular cancer that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells and arises_from the tissues that cover structures located_in the eye.]
obsolete leukemic reticuloendotheliosis of lymph nodes of inguinal region and lower limb	DOID_14258
Down syndrome	DOID_14250	[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.]