Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
J-774 cell	BTO_0002279	[Mouse macrophage cell line.]
bladder urachal adenocarcinoma	MONDO_0004331	[A adenocarcinoma that involves the urachus.]
urachus cancer	MONDO_0001378	[A malignant neoplasm involving the urachus.]
bladder urachal carcinoma	MONDO_0003715	[Urachal cancer is a type of bladder cancer, making up less than 1% of all bladder cancers. The urachus is a structure normally only present during development in the womb that connects the bellybutton and the bladder. This connection normally disappears before birth, but in some people remains. Urachalcancers are usually diagnosed in adults in their 50's and 60's and may develop at the dome or anterior wall of the bladder, along the midline of the body (including the belly button), and between the pubis symphasis and the bladder.Most urachal cancersare adenocarcinomas (cancers that develop from gland cells).Others may besarcomas (which develop from connective tissue -such as leiomyosarcoma, rhabdomyosarcoma, and malignant fibrous histiocytoma), small cell carcinomas, transitional cell cancer, and mixed neoplasias. Most individuals with urachal cancer have symptoms of with hematuria (blood in urine). Other symptoms may include abdominal pain, a palpable abdominal mass, mucinuria, and bacteriuria. Treatment usually involved surgery to remove the cancer.]
129X1/SvJ	EFO_0000600	[129X1/SvJ is a substrain of the mouse strain 129 as described in Jackson Laboratory http://jaxmice.jax.org/strain/000691.html Note this strain was formerly called 129X1]
129 mouse strain	EFO_0000597	[129 is a mouse strain as described in Jackson Laboratory http://www.informatics.jax.org/mgihome/nomen/strain_129.shtml]
ribonucleoside monophosphate biosynthetic process	GO_0009156	[ The chemical reactions and pathways resulting in the formation of a ribonucleoside monophosphate, a compound consisting of a nucleobase linked to a ribose sugar esterified with phosphate on the sugar. ]
nucleoside monophosphate biosynthetic process	GO_0009124	[ The chemical reactions and pathways resulting in the formation of a nucleoside monophosphate, a compound consisting of a nucleobase linked to a deoxyribose or ribose sugar esterified with phosphate on the sugar. ]
ribonucleoside monophosphate metabolic process	GO_0009161	[ The chemical reactions and pathways involving a ribonucleoside monophosphate, a compound consisting of a nucleobase linked to a ribose sugar esterified with phosphate on the sugar. ]
African American	HANCESTRO_0568
gastric intestinal type adenocarcinoma	EFO_0000504	[An adenocarcinoma of the stomach arising on a background of intestinal metaplasia. Microscopically, it is characterized by a glandular pattern and it closely resembles a colonic adenocarcinoma. Grossly, it tends to be nodular, polypoid or ulcerated.]
hydantoin-5-propionic acid	CHEBI_28297	[A imidazolidine-2,4-dione that is hydantoin substituted by a 2-carboxyethyl group at position 4.]
obsolete_gastrointestinal stromal tumor	EFO_0000505	[All tumors in the GASTROINTESTINAL TRACT arising from mesenchymal cells (MESODERM) except those of smooth muscle cells (LEIOMYOMA) or Schwann cells (SCHWANNOMA).]
gene knock out	EFO_0000506
generation	EFO_0000507	[The number of cell passages if the organism or organism part that is cultured is unicellular or a cell culture; otherwise the number of generations.]
inherited	MONDO_0021152	[A characteristic of a disease in which the cause of the disease is a genetic problem inherited from either or both parents.]
obsolete_genetic factor	EFO_0000509
iridocorneal endothelial syndrome	MONDO_0018988	[Iridocorneal endothelial (ICE) syndrome describes a group of progressive corneal proliferative endotheliopathies comprised of Chandler syndrome, Cogan-Reese syndrome and essential iris atrophy, affecting mainly young adult females and characterized by iris holes and atrophy, papillary distortion, anterior synechiae, corneal edema and often with secondary glaucoma and corneal decompensation as complications]
obsolete rare hereditary thrombophilia	MONDO_0016320
Tolosa-Hunt syndrome	MONDO_0018983	[Tolosa-Hunt syndrome is an ophthalmoplegic syndrome, affecting all age groups, characterized by acute attacks (lasting a few days to a few weeks) of periorbital pain, ipsilateral ocular motor nerve palsies, ptosis, disordered eye movements and blurred vision usually caused by a non-specific inflammatory process in the cavernous sinus and superior orbital fissure. It has an unpredicatable course with spontaneous remission occurring in some and recurrence of attacks in others.]