All terms in DOID

Label Id Description
Paramyxoviridae NCBITaxon_11158
fibrochondrogenesis DOID_0060465 [An osteochondrodysplasia that is characterized by shortened long bones in the arms and legs that are unusually wide at the ends, flattened vertebrae with a characteristic pinched or pear shape, and a very narrow chest in infants with short, wide ribs and a round and prominent abdomen.]
Batillus NCBITaxon_133423
Turbo 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 [A synostosis that is characterized by uni- or bilateral fusion of the humerus and radius bones at the elbow level, with or without associated ulnar and carpal/metacarpal deficiency, leading to loss of elbow motion and, in many cases, functional arm incapacity.]
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.]
chromosome 5p13 duplication syndrome DOID_0060460 [A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 5p13 region.]
chromosomal duplication syndrome DOID_0060429 [A chromosomal disease that has_material_basis_in extra copies of a chromosomal region.]
chromosome Xp11.23-p11.22 duplication syndrome DOID_0060461 [A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome Xp11.23-p11.22 region.]
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.]
susceptibility to hepatitis C virus MIM_609532
Rubulavirinae NCBITaxon_2560080
Timothy grass allergy DOID_0060498 [A pollen allergy triggered by Phleum pratense pollen.]
pollen allergy DOID_0060497 [A respiratory allergy triggered by pollen.]