Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
obsolete_hindgut proper primordium	EFO_0003368
9-cis-retinoic acid	CHEBI_50648
bone density conservation agent	CHEBI_50646	[An agent that inhibits bone resorption and/or favor bone mineralization and bone regeneration. Used to heal bone fractures and to treat metabolic bone diseases.]
primordial midbrain channel	UBERON_2005017	[The vessel between the anterior cerebral vein and the mid cerebral vein. Isogai et al. 2001.]
multiple mitochondrial dysfunctions syndrome 4	MONDO_0014611	[Any fatal multiple mitochondrial dysfunctions syndrome in which the cause of the disease is a mutation in the ISCA2 gene.]
IL.00 inflorescence just visible stage	PO_0007006	[An inflorescence detectable phase during which an inflorescence is just visible, but has not yet reach one quarter of its full length. Includes the time when the inflorescence can be seen by removing outer leaves or bracts, or when the inflorescence is visible as a swelling of the outer leaves or bracts, such as booting in Zea. This phase can only be used if the final length of the inflorescence is known.]
A-549 cell	BTO_0000018	[ Human lung carcinoma established from an explanted lung tumor which was removed from a 58-year-old Caucasian man in 1972; cells were described to induce tumors in athymic mice and to synthesize lecithin. ]
early whole plant fruit ripening stage	PO_0007001	[The early stage in fruit ripening.]
whole plant fruit ripening stage	PO_0007010	[Maturation of the fruit.]
chondroblastic osteosarcoma	MONDO_0002627	[An osteosarcoma characterised by the presence of atypical cartilage of variable cellularity. It may or may not be associated with the presence of myxoid areas or focal bone formation.]
obsolete_inclusive hindgut primordium	EFO_0003350
obsolete_foregut primordium	EFO_0003352
(1->3)-beta-D-glucan	CHEBI_37671	["A beta-D-glucan in which the glucose units are connected by (1->3) linkages." []]
induces sterile inflammation	EFO_0004367
small cell osteogenic sarcoma	MONDO_0002630	[An osteosarcoma usually arising from the metaphysis of long bones. It is characterized by the presence of small cells and osteoid production. The prognosis is usually unfavorable.]
obsolete_gnathal primordium	EFO_0003351
obsolete_labial sensory complex primordium	EFO_0003354
obsolete_maxillary sensory complex primordium	EFO_0003353
mandibulofacial dysostosis with alopecia	MONDO_0014608	[A syndrome characterized by malar and mandibular hypoplasia, typically associated with abnormalities of the ears and eyelids, and with alopecia.]
mandibulofacial dysostosis	MONDO_0015483	[A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)]