10 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
| DOID:14566 | disease of cellular proliferation | A disease that is characterized by abnormally rapid cell division. |
| DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
| DOID:863 | nervous system disease | A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system. |
| DOID:331 | central nervous system disease | A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system. |
| DOID:0060085 | organ system benign neoplasm | A benign neoplasm that is classified by the organ system from which it is arising from. |
| DOID:0060072 | benign neoplasm | A disease of cellular proliferation that results in abnormal growths in the body which lack the ability to metastasize. |
| DOID:0060115 | nervous system benign neoplasm | An organ system benign neoplasm that is located_in the central nervous system or located_in the peripheral nervous system. |
| DOID:0060090 | central nervous system benign neoplasm | A nervous system benign neoplasm that is characterized by lack of malignancy. |
| DOID:0081285 | myxoid glioneuronal tumor | A central nervous system benign neoplasm that is characterized by a dinucleotide mutation at codon 385 of the PDGFR gene. It usually occurs in the septum pellucidum but has also been described in the corpus callosum and periventricular white matter of the lateral ventricle. It is composed of oligodendrocyte-like cells in a prominent myxoid stroma. |
9 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0060090 | DOID:0081285 |
| is_a | DOID:14566 | DOID:0081285 |
| is_a | DOID:4 | DOID:0081285 |
| is_a | DOID:863 | DOID:0081285 |
| is_a | DOID:0060085 | DOID:0081285 |
| is_a | DOID:7 | DOID:0081285 |
| is_a | DOID:0060072 | DOID:0081285 |
| is_a | DOID:331 | DOID:0081285 |
| is_a | DOID:0060115 | DOID:0081285 |
