Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
ureteral disease	DOID_1426	[A urinary system disease that is located_in the ureter.]
Abnormality of long bone morphology	HP_0011314	[An abnormality of size or shape of the long bones.]
Adie syndrome	DOID_11549	[A syndrome that is a neurological disorder affecting the pupil of the eye and the autonomic nervous system. It is characterized by one eye with a pupil that is larger than normal and constricts slowly in bright light (tonic pupil), along with the absence of deep tendon reflexes, usually in the Achilles tendon.]
Talaromyces marneffei	NCBITaxon_37727
Talaromyces	NCBITaxon_5094
obsolete Pars plana exudative cyst	DOID_12879
bladder exstrophy-epispadias-cloacal exstrophy complex	DOID_0080173	[A physical disorder that is characterized as a spectrum of anomalies involving the urinary tract, genital tract, musculoskeletal system and sometimes the intestinal tract.]
bladder exstrophy	DOID_0080174	[A bladder exstrophy-epispadias-cloacal exstrophy complex that is characterized by an evaginated bladder plate, epispadias and an anterior defect of the pelvis, pelvic floor and abdominal wall. The rear portion of the bladder wall (posterior vesical wall) turns outward (exstrophy) through an opening in the abdominal wall and urine is excreted through this opening.]
bladder disease	DOID_365	[A urinary system disease that is located_in the bladder.]
urinary bladder	UBERON_0001255
cloacal exstrophy	DOID_0080175	[A bladder exstrophy-epispadias-cloacal exstrophy complex that is characterized by a defect in the urethra, bladder and bowel.]
meningococcal meningitis	DOID_0080176	[A bacterial meningitis that has_material_basis_in Neisseria meningitidis infection.]
Hypodontia	HP_0000668	[A developmental anomaly characterized by a reduced number of teeth, whereby up to 6 teeth are missing.]
Reduced number of teeth	HP_0009804	[The presence of a reduced number of teeth as in Hypodontia or as in Anodontia.]
normophosphatemic familial tumoral calcinosis	DOID_0080170	[A calcinosis that is characterized by massive periarticular, and seldom visceral, deposition of calcified tumors.]
esophageal atresia/tracheoesophageal fistula	DOID_0080171	[A gastrointestinal system disease that is characterized by abnormal development of the esophagus and trachea where the upper esophagus does not connect (atresia) to the lower esophagus and stomach and may also include tracheoesophageal fistula where the esophagus and the trachea are abnormally connected which allows fluids from the esophagus to get into the airways and interfere with breathing.]
thiopurine S-methyltransferase deficiency	DOID_0080172	[An inherited metabolic disease that is characterized by significantly reduced activity of an enzyme that helps the body process drugs called thiopurines.]
obsolete idiopathic urticaria	DOID_12881
oculomotor nerve paralysis	DOID_11550
third cranial nerve disease	DOID_562