Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete fetal distress	DOID_4027
obsolete non-mucinous bronchioloalveolar lung carcinoma	DOID_5358
breast malignant eccrine spiradenoma	DOID_7983	[A breast cancer that arises_from cutaneous sweat glands and is characterized by a focus of benign spiradenoma within or adjacent to the malignant tumor, as evidenced by increased mitotic rate, necrosis, nuclear atypia, pleomorphism, and hyperchromasia, loss of nested and trabecular growth patterns, and absence of a dual cell population.]
diffuse idiopathic skeletal hyperostosis	DOID_6652	[A calcinosis that is the calcification or a bony hardening of ligaments in areas where they attach to your spine.]
sclerosing breast papilloma	DOID_7984	[A breast duct papilloma that is characterized by a central area of scarring and elastosis, derived from an obliterated duct.]
breast duct papilloma	DOID_1626	[An intraductal papillary breast neoplasm that is has_material_basis_in epithelial tissue on papillae of vascularized connective tissue.]
fallopian tube germ cell cancer	DOID_5324	[A fallopian tube cancer that derives_from germ cells.]
obsolete fallopian tube serous tumor	DOID_5323
breast large cell neuroendocrine carcinoma	DOID_6657	[A breast carcinoma that is characterized by large cell size, polygonal shape, low nuclear-cytoplasmic ratio, finely granular eosinophilic cytoplasm, occasionally prominent nucleoli, peripheral palisading, mitosis, and necrosis and in which greater than 50% of the tumor cells are positive for neuroendocrine markers (NSE, chromogranin A, synaptophysin).]
childhood central nervous system immature teratoma	DOID_6654
central nervous system immature teratoma	DOID_6019	[A malignant teratoma that is located_in the central nervous system.]
obsolete Partial recent retinal detachment with single defect	DOID_5326
cerebral falx meningioma	DOID_7986
Roberts syndrome	DOID_5325	[A syndrome characterized by tetraphocomelia, craniofacial anomalies, growth retardation, intellectual disability, and cardiac and renal abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in ESCO2 on chromosome 8p21.1.]
obsolete retinal detachment and defect	DOID_5328
retinal detachment	DOID_5327
pulmonary large cell neuroendocrine carcinoma	DOID_6658
cervical large cell neuroendocrine carcinoma	DOID_6659	[A cervix carcinoma that has_material_basis_in neuroendocrine tissue and is characerized by a diffuse, organoid, trabecular, or cord-like pattern of neoplastic cells with abundant cytoplasm, large nuclei, prominent nucleoli, and a high mitotic rate.]
central nervous system osteosarcoma	DOID_7994
obsolete papillotubular adenocarcinoma	DOID_6663