Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
dCAPS_primer	SO_0001699	[A primer with one or more mismatches to the DNA template corresponding to a position within a restriction enzyme recognition site.]
ribozyme	SO_0000374	[An RNA with catalytic activity.]
enzymatic_RNA	SO_0000372	[An RNA sequence that has catalytic activity with or without an associated ribonucleoprotein.]
recombinationally_inverted_gene	SO_0000373	[A recombinationally rearranged gene by inversion.]
conjugative_transposon	SO_0000371	[A transposon that encodes function required for conjugation.]
trachea leiomyoma	DOID_248	[A respiratory system benign neoplasm that derives_from smooth muscle cells and is located_in the trachea.]
glucocorticoid-induced osteoporosis	DOID_0060343	[An osteoporosis caused by chronic glucocorticoid use. Glucocorticoids impair the replication, differentiation and function of osteoblasts and induce the apoptosis of mature osteoblasts and osteocytes; the also favor osteoclastogenesis leading to an increase in bone resorption.]
acromelic frontonasal dysostosis	DOID_0060342	[A dysostosis characterized by cranium bifidum, severe hypertelorism, median cleft lip and palate, nasal bifurcation, brachycephaly, large fontanelle, tibial hemimelia, preaxial polydactyly of the feet and brain malformations.]
agnathia-otocephaly complex	DOID_0060341	[A physical disorder characterized by mandibular hypoplasia or agnathia, ventromedial auricular malposition (melotia) and/or auricular fusion (synotia), and microstomia with oroglossal hypoplasia or aglossia. Holoprosencephaly is the most commonly identified association, but skeletal, genitourinary and cardiovascular anomalies and situs inversus have been reported.]
orofaciodigital syndrome VIII	DOID_0060378	[An orofaciodigital syndrome that is characterized by tongue lobulation, hypoplasia of the epiglottis, cleft lip, polydactyly, short stature and intellectual deficit, and has_material_basis_in X-linked recessive inheritance.]
orofaciodigital syndrome VII	DOID_0060377	[An orofaciodigital syndrome that is characterized by oral, facial and digital abnormalities, and has_material_basis_in autosomal dominant inheritance.]
three_prime_restriction_enzyme_junction	SO_0001690
single_strand_restriction_enzyme_cleavage_site	SO_0001694	[A restriction enzyme cleavage site whereby only one strand is cut.]
blunt_end_restriction_enzyme_cleavage_site	SO_0001691	[A restriction enzyme recognition site that, when cleaved, results in no overhangs.]
restriction_enzyme_recognition_site	SO_0001687	[The nucleotide region (usually a palindrome) that is recognized by a restriction enzyme. This may or may not be equal to the restriction enzyme binding site.]
floxed	SO_0000359	[An attribute describing sequence that is flanked by Lox-P sites.]
flanked	SO_0000357	[An attribute describing a region that is bounded either side by a particular kind of region.]
blunt_end_restriction_enzyme_cleavage_junction	SO_0001693	[A restriction enzyme cleavage site where both strands are cut at the same position.]
restriction_enzyme_cleavage_junction	SO_0001688	[The boundary at which a restriction enzyme breaks the nucleotide sequence.]
RNA	SO_0000356	[An attribute describing a sequence consisting of nucleobases bound to a repeating unit made of a D-ribose ring connected to a phosphate backbone.]