Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
Riboviria	NCBITaxon_2559587
fibrochondrogenesis	DOID_0060465
Batillus	NCBITaxon_133423
Turbo <genus>	NCBITaxon_63672
gingival fibromatosis	DOID_0060466	[A gingival overgrowth characterized by benign, slowly progressive, nonhemorrhagic, fibrous enlargement of the oral masticatory mucosa.]
gingival overgrowth	DOID_3086
humeroradial synostosis	DOID_0060467
synostosis	DOID_11971	[A dysostosis that results_in abnormal fusing of adjacent bones.]
Holt-Oram syndrome	DOID_0060468	[A syndrome characterized by congenital anomalies located_in heart and located_in upper limb.]
Miller-Dieker lissencephaly syndrome	DOID_0060469	[A syndrome characterized by classical lissencephaly and distinct facial features and has_material_basis_in submicroscopic deletions of 17p13.3, including the LIS1 gene.]
polypeptide_tungsten_ion_contact_site	SO_0001102	[A binding site that, in the polypeptide molecule, interacts selectively and non-covalently with tungsten ions.]
polypeptide_nickel_ion_contact_site	SO_0001101	[A binding site that, in the polypeptide molecule, interacts selectively and non-covalently with nickel ions.]
polypeptide_molybdenum_ion_contact_site	SO_0001100	[A binding site that, in the polypeptide molecule, interacts selectively and non-covalently with molybdenum ions.]
chromosome 5p13 duplication syndrome	DOID_0060460
chromosomal duplication syndrome	DOID_0060429
chromosome Xp11.23-p11.22 duplication syndrome	DOID_0060461
Desbuquois dysplasia	DOID_0060462	[An osteochondrodysplasia characterized by short stature, joint laxity, scoliosis, and advanced carpal ossification with a delta phalanx.]
NUT midline carcinoma	DOID_0060463	[A carcinoma that is characterized by a BRD4-NUT translocation involving the rearrangement of the bromodomain-containing protein 4 (BRD4) and the gene encoding nuclear protein of the testis (NUT) at 15q14, BRD4-NUT t(15;19)(q14;q13.1) and arises from midline epithelial structures, most commonly the head, neck, and mediastinum.]
Feingold syndrome	DOID_0060464	[A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation.]
Timothy grass allergy	DOID_0060498	[A pollen allergy triggered by Phleum pratense pollen.]