Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
salivary gland body primordium	FBbt_00005512	[Primordium that will form the secretory body of the embryonic/larval salivary gland. This primordium is first apparent as two epidermal placodes on the medial surface of the labial buds during stage 11. These placodes invaginate during embryonic stage 11 to form simple tubes on each side of the embryo that are positioned approximately along the dorso-ventral axis. Once internalized, the primordia migrate posteriorly during embryonic stage 12. They fuse to the developing salivary gland common duct by stage 13 and shortly after begin to show signs of secretory activity.]
caesium chloride	CHEBI_63039	["The inorganic chloride salt of caesium; each caesium ion is coordinated by eight chlorine ions." []]
phase-transfer catalyst role	CHEBI_63060
vasoconstrictor agent	CHEBI_50514	[Drug used to cause constriction of the blood vessels.]
infantile hypertrophic cardiomyopathy due to MRPL44 deficiency	MONDO_0014162	[Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency is a rare mitochondrial oxidative phosphorylation disorder with complex I and IV deficiency characterized by hypertrophic cardiomyopathy, hepatic steatosis with elevated liver transaminases, exercise intolerance and muscle weakness. Neuro-opthalmological features (hemiplegic migraine, Leigh-like lesions on brain MRI, pigmentary retinopathy) have been reported later in life.]
ammonium nitrate	CHEBI_63038	["The ammonium salt of nitric acid." []]
fertilizer	CHEBI_33287
explosive role	CHEBI_63490	[A substance capable of undergoing rapid and highly exothermic decomposition.]
TCR-alpha-beta-positive T-cell deficiency	MONDO_0014160	[A non-severe combined immunodeficiency disorder manifesting with recurrent respiratory infections, candidiasis, diarrhea, and failure to thrive. Patients show a clear predisposition to herpes viral infections, and features of immune dysregulation, including hypereosinophilia, vitiligo, and alopecia areata. Other features include lymphadenopathy and hepatosplenomegaly. CD3+ T-cells express TCR- gamma\|delta, but little or no TCR-alpha\|beta.]
Ruminococcus	NCBITaxon_1263
Drosophila developmental tissue	EFO_0003333
somatic muscle primordium	FBbt_00005518	[Primordium of the embryonic/larval somatic musculature. It arises from the outer layer of the mesoderm. During germ band shortening (stage 13), it segregates into loose segmental clusters. Within these clusters, muscle formation proceeds by fusion of fusion competent myoblasts to muscle founder cells. Formation of the embryonic/larval somatic musculature is complete by stage 17.]
multiple congenital anomalies-hypotonia-seizures syndrome 3	MONDO_0014165	[Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome is a rare congenital disorder of glycosylation characterized by neonatal hypotonia, global development delay, developmental regress and severe to profound intellectual disability, infantile onset seizures that are initially associated with febrile episodes with subsequent transition to unprovoked seizures, impaired vision with esotropia and nystagmus, progressive cerebral and cerebellar atrophy, skeletal abnormalities (including brachycephaly, scoliosis, slender long bones, delayed bone age, pectus excavatum and osteopenia), inverted nipples and dysmorphic features including high and narrow forehead, frontal bossing, short nose, depressed nasal bridge, anteverted nares, high palate and wide open mouth consistent with facial hypotonia. Other features may include cardiac abnormalities (such as patent ductus arteriosus, atrial septal defects), urogenital abnormalities (such as nephrocalcinosis, urolithiasis), and low plasma concentration of alkaline phosphatase.]
slender bone dysplasia	MONDO_0019699
multiple congenital anomalies-hypotonia-seizures syndrome	MONDO_0100247
Pediococcus pentosaceus	NCBITaxon_1255
Pediococcus acidilactici	NCBITaxon_1254
bone remodeling disease	MONDO_0000833	[A bone disease that results in formation or resorption abnormalities located in bone.]
vulvar disease	MONDO_0002187	[A non-neoplastic or neoplastic disorder that affects the vulva. Representative examples include infection, Bartholin gland adenoma, and vulvar carcinoma.]
F13	EFO_0002711