All terms in DOID

Label Id Description
pituicytoma DOID_0081280 [A posterior pituitary gland neoplasm that is characterized by the presence of elongated, spindle-shaped neoplastic glial cells that form storiform patterns or interlacing fascicular arrangements.]
posterior pituitary gland neoplasm DOID_5048 [A pituitary gland benign neoplasm that arises from the neurohypophysis.]
oligodendroglioma, IDH-mutant and 1p/19q-codeleted grade 2 DOID_0081281 [An IDH-mutant, and 1p/19q-codeleted oligodendroglioma that is characterized as a well differentiated tumor lacking anaplastic features (brisk mitotic activity, microvascular proliferation, necrosis).]
IDH-mutant and 1p/19q-codeleted oligodendroglioma DOID_0080882 [An anaplastic oligodendroglioma that has_material_basis_in IDH gene family mutation and combined whole-arm losses of 1p and 19q (1p/19q codeletion).]
oligodendroglioma, IDH-mutant and 1p/19q-codeleted, grade 3 DOID_0081282 [An IDH-mutant, and 1p/19q-codeleted oligodendroglioma that is characterized as grade 3 tumors associated with a more rapid growth. Grade 3 tumors appear to have abnormalities on chromosomes 9 or 10, along with unusual amounts of growth factors and proteins, which are thought to contribute to the more rapid growth of these gliomas.]
papillary glioneuronal tumor DOID_0081283 [A central nervous system benign neoplasm that is characterized by the presence of astrocytes that line vascular and hyalinized pseudopapillae.]
food storage organ UBERON_0010039
desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma DOID_0081259 [A ganglioglioma occurring predominantly in the cerebral hemispheres of infants, that are driven by MAPK pathway activation and composed of a mixed astrocytic and neuronal component (DIG) or an astrocytic component only (DIA) embedded in an extensive desmoplastic stroma, often containing foci of undifferentiated embryonal-like tumour cells.]
ganglioglioma DOID_5078 [A cell type benign neoplasm that has_material_basis_in glial-type cells.]
posterior fossa group B ependymoma DOID_0081255 [A posterior fossa ependymoma that arises in the posterior fossa with characteristic DNA methylation patterns including retention of nuclear H3 p.K28me3 (K27me3) expression, absence of CpG island hypermethylation, absence of global DNA hypomethylation, and absence of EZHIP overexpression.]
posterior fossa ependymoma DOID_0080889 [A high grade ependymoma that is located within the posterior fossa.]
astrocytoma, IDH-mutant, grade 2 DOID_0081256 [An IDH-mutant anaplastic astrocytoma that is characterized by the presence of well-differentiated fibrillary glial cells diffusely infiltrating the central nervous system.]
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.]