All terms in DOID

Label Id Description
obsolete ovarian dermoid cyst with angiosarcoma DOID_6632
ovarian clear cell adenocarcinoma DOID_5304 [A ovarian adenocarcinoma that derives_from epithelial cells which have clear cytoplasm.]
cervical clear cell adenocarcinoma DOID_5303 [A cervical adenocarcinoma that derives_from epithelial cells which have clear cytoplasm.]
diffuse glioma, H3 G34 mutant DOID_0080880 [A histone mutated tumor that has_material_basis_in mutations in codon 34 of the H3 histone family 3A protein.]
nested variant infiltrating bladder urothelial carcinoma DOID_7969
organic heterobicyclic compound CHEBI_27171
childhood CNS choriocarcinoma DOID_6639 [A choriocarcinoma characterized by extraembryonic differentiation along trophoblastic lines and high serum and CSF levels of HCG/_-HCG, has_material_basis_in abnormally proliferating cells, derives_from germ cells.]
obsolete malignant ovarian clear cell neoplasm DOID_5305
ampulla of Vater clear cell adenocarcinoma DOID_5308
lipid-cell variant infiltrating bladder urothelial carcinoma DOID_7967
plasmacytoid variant infiltrating bladder urothelial carcinoma DOID_7968
urethra clear cell adenocarcinoma DOID_5307 [A clear cell adenocarcinoma that is located_in the urethra.]
non-syndromic X-linked intellectual disability 96 DOID_0112035 [A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability that has_material_basis_in hemizygous mutation in SYP on chromosome Xp11.23.]
pericytoma with t(7;12) DOID_0080896 [A perivascular tumor that is characterized by a perivascular pattern of spindle-to-ovoid cell proliferation and that has_material_basis_in t(7;12)(p22;q13) translocation with resultant ACTB-GLI1 fusion.]
non-syndromic X-linked intellectual disability 9 DOID_0112034 [A non-syndromic X-linked intellectual disability characterized by nonprogressive intellectual disability that has_material_basis_in hemizygous mutation in the FTSJ1 gene on chromosome Xp11.23.]
solitary fibrous tumor/hemangiopericytoma DOID_0080897 [A connective tissue cancer that is characterized as the combination of solitary fibrous tumors and hemangiopericytomas.]
non-syndromic X-linked intellectual disability 81 DOID_0112033 [A non-syndromic X-linked intellectual disability characterized by moderate to severe intellectual disability that has_material_basis_in hemizygous mutation in a region on chromosome Xp11.2-q12.]
cerebellofaciodental syndrome DOID_0080898 [A syndrome that is characterized by delayed development, intellectual disability, abnormal facial and dental findings, and cerebellar hypoplasia and that has_material_basis_in homozygous or compound heterozygous mutation in the BRF1 gene on chromosome 14q32.]
non-syndromic X-linked intellectual disability 92 DOID_0112032 [A non-syndromic X-linked intellectual disability characterized by moderate to severe intellectual disability that has_material_basis_in hemizygous mutation in a region on chromosome Xp11.3.]
lung pleomorphic carcinoma DOID_0080899 [A pleomorphic carcinoma that is characterized by the presence of malignant glandular or squamous cells associated with malignant giant and spindle cells and that is located_in the lung.]