Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
severe headache	SYMP_0000130
headache	SYMP_0000504	[Headache is a pain characterized by a pain in the head.]
extracutaneous mastocytoma	DOID_4659
systemic mastocytosis	DOID_349
mast cell neoplasm	DOID_3664	[A hematologic cancer that has_material_basis_in mast cells.]
partial motor epilepsy	DOID_3327
focal epilepsy	DOID_2234	[An epilepsy syndrome that is characterised by seizures that are preceded by an isolated disturbance of a cerebral function and arise from an epileptic focus, a small portion of the brain that serves as the irritant driving the epileptic response.]
severe joint pain	SYMP_0000131
joint pain	SYMP_0000064
temporal lobe epilepsy	DOID_3328
obsolete clear cell myomelanocytic tumor of the Falciform Ligament/Ligamentum Teres	DOID_5989
benign mastocytoma	DOID_4658
cell type benign neoplasm	DOID_0060084	[A benign neoplasm that is classified by the type of cell or tissue from which it is derived.]
Burkholderia	NCBITaxon_32008
Burkholderiaceae	NCBITaxon_119060
copy_number_variation	SO_0001019	[A variation that increases or decreases the copy number of a given region.]
sequence_length_alteration	SO_0000248	[A kind of kind of sequence alteration where the copies of a region present varies across a population.]
epitope	SO_0001018	[A binding site that, in the molecule, interacts selectively and non-covalently with antibodies, B cells or T cells.]
binding_site	SO_0000409	[A biological_region of sequence that, in the molecule, interacts selectively and non-covalently with other molecules. A region on the surface of a molecule that may interact with another molecule. When applied to polypeptides: Amino acids involved in binding or interactions. It can also apply to an amino acid bond which is represented by the positions of the two flanking amino acids.]
silent_mutation	SO_0001017	[A sequence variant that does not affect protein function. Silent mutations may occur in genic ( CDS, UTR, intron etc) and intergenic regions. Silent mutations may have affects on processes such as splicing and regulation.]