All terms in DOID

Label Id Description
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.]
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.]
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 the ESCO2 gene 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 characterized by a diffuse, organoid, trabecular, or cord-like pattern of neoplastic cells with abundant cytoplasm, large nuclei, prominent nucleoli, and a high mitotic rate.]
autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques DOID_0112013 [A mutilating palmoplantar keratoderma with periorificial keratotic plaques that has_material_basis_in heterozygous mutation in the TRPV3 gene on chromosome 17p13.2.]
mutilating palmoplantar keratoderma with periorificial keratotic plaques DOID_0112011 [A keratosis characterized by a bilateral mutilating palmoplantar keratoderma and periorificial keratotic plaques with severe pruritus of lesions.]
X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques DOID_0112012 [A mutilating palmoplantar keratoderma with periorificial keratotic plaques that has_material_basis_in hemizygous mutation in the MBTPS2 gene on chromosome Xp22.12.]
pituitary adenoma 3 DOID_0112010 [A pituitary adenoma characterized by development of predominantly GH-secreting pituitary adenomas but also in some patients ACTH-secreting adenomas that has_material_basis_in somatic mutation in the GNAS gene on chromosome 20q13.32.]