All terms in DOID

Label Id Description
IDH-mutant anaplastic astrocytoma DOID_0080875 [An anaplastic astrocytoma carrying IDH mutations.]
astrocytoma, IDH-mutant, grade 3 DOID_0081257 [An IDH-mutant anaplastic astrocytoma that is characterized by the presence of increased mitotic activity and anaplastic features.]
prepuce UBERON_0011374
papillary tumor of the pineal region DOID_0081251 [A pineal gland cancer that is characterized by the presence of neuroepithelial cells and a papillary architecture.]
pineal gland cancer DOID_5032 [An endocrine gland located_in the pineal gland located in the brain.]
supratentorial ependymoma, ZFTA fusion–positive DOID_0081252 [A suptratentorial ependymoma that is characterized by the presence of a fusion gene involving ZFTA gene.]
supratentorial ependymoma DOID_0080890 [A high grade ependymoma that is located within the supratentorial brain.]
supratentorial ependymoma, YAP1 fusion–positive DOID_0081253 [A supratentorial ependymoma that is characterized by the presence of a fusion gene involving YAP1 gene.]
posterior fossa group A ependymoma DOID_0081254 [A posterior fossa ependymoma that arises in the posterior fossa with characteristic DNA methylation patterns, including CpG island hypermethylation, global DNA hypomethylation, reduction of nuclear H3 p.K28me3 (K27me3) expression, and EZHIP overexpression.]
oral gland UBERON_0010047
gland of digestive tract UBERON_0003408
gland UBERON_0002530
CIC-rearranged sarcoma DOID_0081250 [An EWSERI-negative small round cell tumor that is characterized by a recurrent translocation involving the CIC gene on chromosome 19 and either DUX4 gene on chromosome 4 or DUX4L gene on chromosome 10. The translocation results in either CIC-DUX4, t(4;19)(q35;q13) or CIC-DUX4L, t(10;19)(q26;q13) fusions.]
EWSR1-negative small round cell tumor DOID_0081249 [A small cell sarcoma that is characterized by the absence of EWSR1 rearrangement and the presence of small round malignant cells with a small amount of cytoplasm.]
pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures DOID_0081266 [A lissencephaly that is characterized by progressive microcephaly associated with abnormal facial features, hypotonia, and variable global developmental delay with impaired intellectual development and that has_material_basis_in homozygous or compound heterozygous mutation in the TUBGCP2 gene on chromosome 10q26.]
graft-versus-host disease DOID_0081267 [An immune system disease that is characterized by recognition by mature donor T cells, that contaminate the allogeneic bone marrow, of the recipient's tissue as foreign, causing a severe inflammatory disease characterized by rashes, diarrhea, and liver disease, and that has_material_basis_in an associated with variation in the interleukin-10 gene (IL10) on chromosome 1q32.]
pulmonary venoocclusive disease 1 DOID_0081268 [A pulmonary venoocclusive disease that has_material_basis_in heterozygous mutation in the BMPR2 gene on chromosome 2q33.]
pulmonary venoocclusive disease DOID_5453 [A pulmonary hypertension that is characterized by pulmonary venous constriction or occlusion, resulting in pulmonary hypertension.]
pulmonary venoocclusive disease 2 DOID_0081269 [A pulmonary venoocclusive disease that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2AK4 gene on chromosome 15q15 and that is characterized histologically by widespread fibrous intimal proliferation of septal veins and preseptal venules, and is frequently associated with pulmonary capillary dilatation and proliferation.]
Candida NCBITaxon_5475