Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
Melampsora larici-populina	NCBITaxon_203908
Candidatus Blochmannia floridanus	NCBITaxon_203907
xanthine	CHEBI_15318	[A purine nucleobase found in humans and other organisms.]
obsolete_Potocki-Shaffer syndrome	Orphanet_52022
Dehalococcoides	NCBITaxon_61434
butyrate	CHEBI_17968
glutarate(2-)	CHEBI_30921	[A dicarboxylic acid dianion obtained by deprotonation of both the carboxy groups of glutaric acid]
3-hydroxy-3-methylglutarate(1-)	CHEBI_30920	[A dicarboxylic acid monoanion resulting from the removal of a proton from one of the carboxylic acid groups of 3-hydroxy-3-methylglutaric acid.]
Fusarium anthophilum	NCBITaxon_48485
GM15227	CLO_0027473	[DNA POLYMORPHISM DISCOVERY RESOURCE COLLECTION]
GM15236	CLO_0027467	[DNA POLYMORPHISM DISCOVERY RESOURCE COLLECTION]
Montastraea faveolata	NCBITaxon_48498
Ulnar/fibula ray defect - brachydactyly	Orphanet_52056	[Ulnar/fibula ray defect - brachydactyly syndrome is a very rare malformation syndrome characterized by ulnar hypoplasia associated with hypoplastic to absent fourth and/or fifth digits, fibular hypoplasia, short stature and facial dysmorphism.]
puromycin	CHEBI_17939	[An aminonucleoside antibiotic, derived from the Streptomyces alboniger bacterium, that causes premature chain termination during translation taking place in the ribosome., A monounsaturated very long-chain fatty acid with a 22-carbon backbone and a single double bond originating from the 9th position from the methyl end, with the double bond in the trans- configuration.]
Craniosynostosis - intracranial calcifications	Orphanet_52054	[Craniosynostosis - intracranial calcifications is a rare syndromic craniosynostosis with unknown etiology characterized by variable degrees of craniosynostosis and basal ganglia calcifications with the inconsistent association of mild dysmorphic facies with prominent eyes and nasal bridge. Intelligence is not affected. Craniosynostosis - intracranial calcifications appears to be transmitted in an autosomal recessive manner.]
Agenesis of the corpus callosum - intellectual disability - coloboma - micrognathia	Orphanet_52055	[Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia syndrome is a developmental anomalies syndrome characterized by coloboma of the iris and optic nerve, facial dysmorphism, intellectual deficit, agenesis of the corpus callosum (ACC), sensorineural hearing loss, skeletal anomalies and short stature.]
inguinal part of abdomen	UBERON_0008337	[The external junctural region between the lower part of the abdomen and the thigh.]
aldosterone secretion	GO_0035932	[The regulated release of aldosterone into the circulatory system. Aldosterone is a pregnane-based steroid hormone produced by the outer-section (zona glomerulosa) of the adrenal cortex in the adrenal gland, and acts on the distal tubules and collecting ducts of the kidney to cause the conservation of sodium, secretion of potassium, increased water retention, and increased blood pressure. The overall effect of aldosterone is to increase reabsorption of ions and water in the kidney.]
N(omega),N(omega)-dimethyl-L-arginine	CHEBI_17929	[Encoded by HOXC6 Gene (ANTP Family), 153- and 235-amino acid (27-kD) Homeobox C6 Protein isoforms are highly conserved sequence-specific DNA-binding homeobox transcription repressors that can cooperate with other HOX proteins and may contribute to the breast cell phenotype through co-operative interactions. As part of a developmental regulatory system that provides anterior-posterior positional identity to cells, HOXC6 may regulate the coordinated expression of multiple genes involved in morphogenesis and differentiation. (from LocusLink, Swiss-Prot, OMIM, and NCI), A methyl-L-arginine having two methyl groups both attached to the primary amino moiety of the guanidino group., A L-arginine derivative having two methyl groups both attached to the primary amino moiety of the guanidino group., Homeobox protein Hox-C6 (235 aa, ~27 kDa) is encoded by the human HOXC6 gene. This protein plays a role in transcription and embryonic development., A methyl-L-arginine that has formula C8H18N4O2.]
GM15242	CLO_0027447	[CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 9; CYP2C9 DNA POLYMORPHISM DISCOVERY RESOURCE COLLECTION]