Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
obsolete_intercostal muscle	EFO_0001368	[A muscle located between two ribs.]
indole-3-acetate	CHEBI_30854	[An indol-3-yl carboxylic acid anion that is the conjugate base of indole-3-acetic acid.]
6alpha-methylprednisolone	CHEBI_6888
Dahl salt-sensitive	EFO_0001350
Sprague Dawley	EFO_0001352
WKY	EFO_0001351
SALK_037727	EFO_0001354	[SALK_037727 is an Arabidopsis thaliana strain as described in TAIR http://www.arabidopsis.org/servlets/TairObject?type=germplasm&id=4640315]
obsolete_multiple endocrine neoplasia	Orphanet_276161
Lewis	EFO_0001353
taurolithocholic acid sulfate	CHEBI_17864	[The steroid sulfate of taurolithocholic acid.]
neurotic disorder	EFO_0004257	[A form of functional mental illness that manifests in distressed emotional reactions such as anxiety, obsessive thoughts, compulsive behaviors, or irrational fears., Disorders in which the symptoms are distressing to the individual and recognized by him or her as being unacceptable. Social relationships may be greatly affected but usually remain within acceptable limits. The disturbance is relatively enduring or recurrent without treatment.]
4-methyl-2-oxopentanoate	CHEBI_17865	[A 2-oxo monocarboxylic acid anion that is the conjugate base of 4-methyl-2-oxopentanoic acid.]
sporadic amyotrophic lateral sclerosis	EFO_0001357	[Sporadic amyotrophic lateral sclerosis is a amyotrophic lateral sclerosis in which there is no known cause, such as no family history.]
obsolete_type I diabetes mellitus	EFO_0001359	[An autoimmune disease of endocrine system and is_a diabetes mellitus that results from autoimmune destruction of insulin-producing beta cells of the pancreas., A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence., Diabetes mellitus characterized by insulin deficiency, sudden onset, severe hyperglycemia, rapid progression to ketoacidosis, and death unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence.]
obsolete_Omenn syndrome	Orphanet_39041	[Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; see this term).]
Candidatus Pelagibacter ubique HTCC1062	NCBITaxon_335992
plantaris	UBERON_0011905	[Plantaris is a vestigial structure and one of the superficial muscles of the posterior crural compartment of the leg. It is innervated by the tibial nerve (S1, S2) . It is composed of a thin muscle belly and a long thin tendon. It is approximately 2-4 inches long, and is absent in 7 - 10% of the human population. It is one of the plantar flexors in the superior compartment of the leg along with the gastrocnemius, and soleus. The plantaris is considered an unimportant muscle, it mainly acts with gastrocnemius[WP].]
hindlimb muscle	UBERON_0003663	[Any muscle organ that is part of a hindlimb [Automatically generated definition].]
obsolete_Peyer's patch	EFO_0001381	[Any of numerous large oval patches of closely aggregated nodules of lymphoid tissue in the walls of the small intestine esp. in the ileum that partially or entirely disappear in advanced life and in typhoid fever become the seat of ulcers which may perforate the intestines., Any of numerous large oval patches of closely aggregated nodules of lymphoid tissue in the walls of the small intestine especially in the ileum that partially or entirely disappear in advanced life and in typhoid fever become the seat of ulcers which may perforate the intestines.]
orotate	CHEBI_30839	[2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylate, orotate]