Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
tumor grade 2 or 3, general grading system	MONDO_0024496	[A morphologic qualifier indicating that a neoplastic lesion is moderately to poorly differentiated.]
obsolete_thoracolaryngopelvic dysplasia	Orphanet_3317
obsolete_Thomas syndrome	Orphanet_3316
obsolete_thiopurine S-methyltransferase deficiency	Orphanet_3315
Francisella tularensis subsp. holarctica LVS	NCBITaxon_376619
obsolete_Thiemann disease, familial form	Orphanet_3314	[Thiemann disease is a very rare genetic necrotic bone disorder characterized clinically by painless swelling of the proximal interphalangeal joints associated with osteonecrosis of epiphyses followed by osteoarthritic changes, with onset before 25 years of age and often a benign course.]
N-acetylneuraminate	CHEBI_35418	[A ketoaldonate that is the conjugate base of N-acetylneuraminic acid, obtained by deprotonation of the carboxy group.]
posterior ceratohyal	UBERON_2000627	[Replacement bone that is bilaterally paired and articulates anteriorly with the anterior ceratohyal.]
ventral hyoid arch skeleton	UBERON_0011153
Thrombocytopenia - Robin sequence	Orphanet_3323
obsolete_Hoyeraal-Hreidarsson syndrome	Orphanet_3322	[Hoyeraal-Hreidarsson syndrome (HHS) is a very rare X-linked recessive disorder considered to be a severe variant of dyskeratosis congenita (see this term) characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia.]
tumor grading characteristic	MONDO_0024488	[A modifier that can be applied to a tumor class describing abnormal tumor histology or morphology. It is an indicator of how quickly a tumor is likely to grow and spread]
Thrombocytopenia - absent radius	Orphanet_3320
Tibial aplasia - ectrodactyly	Orphanet_3329
Absent tibia - polydactyly - arachnoid cyst	Orphanet_3328	[Tibia absent - polydactyly - arachnoid cyst syndrome is a very rare constellation of multiple anomalies, including absence or hypoplasia of the tibia.]
obsolete_thyrocerebrorenal syndrome	Orphanet_3327
eccrine sweat gland hamartoma	MONDO_0024482	[A hamartoma characterized by localized eccrine sweat gland malformation.]
obsolete_thymic-renal-anal-lung dysplasia	Orphanet_3326
obsolete_familial thrombomodulin anomalies	Orphanet_3324
upper digestive tract	UBERON_0004908	[The region of the digestive tract extending from the mouth cavity through pharynx esophagus stomach and duodenum.]