Terminology Service < Semantic Lookup Platform

All terms in BAO

Label	Id	Description
Laurence-Moon syndrome	DOID_1930
lysate array	BAO_0000474	[This contains complex samples, such as cell or tissue lysates, spotted on an array surface and interrogated with antibodies.]
small molecule array	BAO_0000473	[Small molecules which are either natural or synthetic are immobilized by robotic printing on a solid support, such as a functionalized glass slide. Protein targets either purified or from a lysate are hybridized to the immobilized small molecules in an attempt to identify the natural ligands for proteins, and also molecules that could regulate their function.]
array	BAO_0000514	[The immobilization of thousands of small molecules, genes or proteins on a glass slide for performing binding studies.]
carbon nanotube based sensor	BAO_0000471	[Carbon nanotubes (CNT) are rolled up seamless cylinders of graphene sheets, exhibiting many unique physical, mechanical and chemical properties. CNT based biosensors are used to detect protein interactions, e.g. protein-DNA, antibody-aptamer interaction, etc.]
protein conformation assessment	BAO_0000470	[This technology relates to measurement of protein conformational properties using one of the following methods: circular dichroism spectroscopy, thermal shift, fluorescence resonance energy transfer (FRET), nuclear magnetic resonance (NMR), X-ray crystallography, etc.]
arterial tortuosity syndrome	DOID_0050645	[A connective tissue disease that is characterized by elongation and generalized tortuosity of the major arteries including the aorta.]
arterial calcification of infancy	DOID_0050644	[A vascular disease that is characterized by generalized calcification of the arterial internal elastic lamina, leading to rupture of the lamina and occlusive changes in the tunica intima with stenosis and decreased elasticity of the vessel wall.]
Arts syndrome	DOID_0050647	[An X-linked disease that is characterized by profound congenital sensorineural hearing impairment, early-onset hypotonia, delayed motor development, mild to moderate intellectual disability, ataxia, and increased risk of infection and has_material_basis_in mutations of the PRPS1 gene.]
Bardet-Biedl syndrome	DOID_1935	[An autosomal recessive disease that results from mutations in multiple BBS genes affecting cellular cilia structure or function (ciliopathy) resulting in variable presentation and characterized principally by obesity, retinitis pigmentosa,vision loss, polydactyly, mental retardation, hypogonadism, and renal failure in some cases.]
distal arthrogryposis	DOID_0050646	[A muscle tissue disease characterized by congenital joint contractures of hand and feet.]
koff	BAO_0000479	[The off-rate associated with the release of inhibitor from an enzyme-inhibitor complex.]
atransferrinemia	DOID_0050649
Rubinstein-Taybi syndrome	DOID_1933	[An autosomal dominant disease characterized by short stature, moderate to sever intellectual disability, distinctive facial features and broad thumbs and first toes; additionally it can include eye abnormalities, heart and kidney defects, dental problems and obesity.]
atelosteogenesis	DOID_0050648
Angelman syndrome	DOID_1932
km	BAO_0000477	[The concentration of substrate at ½ Vmax, according to the Henri-Michaelis-Menten kinetic model. ]
ophthalmoplegia	DOID_539
blood group incompatibility	DOID_4176
Rh isoimmunization	DOID_4175