Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
Anti-herpes simplex virus 2 IgG measurement	EFO_0009350	[Quantification of the IgG antibody isotype produced in response to herpes simplex virus 2 infection]
Leishmania infantum	NCBITaxon_5671
Anti-varicella zoster virus IgG measurement	EFO_0009351	[Quantification of the IgG antibody isotype produced in response to varicella zoster virus infection]
Anti-Helicobacter pylori IgG measurement	EFO_0009352	[Quantification of the IgG antibody isotype produced in response to Helicobacter pylori infection]
hypogonadotropic hypogonadism	MONDO_0018555	[Abnormal ovarian or testicular function due to insufficient hormonal stimulation from the hypothalamic-pituitary axis.]
hypogonadism	MONDO_0002146	[A disorder characterized by decreased function of the gonads. Clinical manifestations in both males and females include poor libido, infertility, and osteoporosis. Additional signs in males include erectile dysfunction, muscle atrophy, gynecomastia and increased abdominal fat. In females, additional signs include shrinking of the breasts and loss of, or failure to develop menstruation.]
FVC change measurement	EFO_0010339	[Quantification of the rate of change in forced vital capacity of an individual over the course of time, used as an indicator of improvement or decay of pulmonary function.]
spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder	MONDO_0018550
hereditary motor and sensory neuropathy	MONDO_0015358	[A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-Tooth DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)]
eye degenerative disorder	MONDO_0004884	[A neurodegenerative disease that involves the eye.]
facial paralysis	MONDO_0001835	[Severe or complete loss of facial muscle motor function. This condition may result from central or peripheral lesions. Damage to CNS motor pathways from the cerebral cortex to the facial nuclei in the pons leads to facial weakness that generally spares the forehead muscles. facial nerve diseases generally results in generalized hemifacial weakness. neuromuscular junction diseases and muscular diseases may also cause facial paralysis or paresis.]
syndromic hereditary optic neuropathy	MONDO_0018609	[A hereditary optic neuropathy that is part of a larger syndrome.]
autosomal recessive complex spastic paraplegia	MONDO_0015089	[Autosomal recessive form of complex hereditary spastic paraplegia.]
dexibuprofen	CHEBI_43415
ventral diencephalon volume measurement	EFO_0010337	[Quantification of the volume of the ventral diencephalon.]
obsolete_follicular lymphoma	EFO_0010338	[Follicular lymphoma is a form of non-Hodgkin lymphoma (see this term) characterized by a proliferation of B cells whose nodular structure of follicular architecture is preserved.]
cholesteryl ester 18:3 measurement	EFO_0010346	[The quantification of cholesteryl ester 18:3 levels in a sample.]
Anti-rubella virus IgG measurement	EFO_0009357	[Quantification of the IgG antibody isotype produced in response to rubella virus infection]
Anti-hepatitis B virus surface antigen IgG measurement	EFO_0009358	[Quantification of antibodies to the hepatitis B virus surface antigen]
cholesteryl ester 20:3 measurement	EFO_0010347	[The quantification of cholesteryl ester 20:3 levels in a sample.]