15 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:0050686 | organ system cancer | A cancer that is classified based on the organ it starts in. |
| DOID:162 | cancer | A disease of cellular proliferation that is malignant and primary, characterized by uncontrolled cellular proliferation, local cell invasion and metastasis. |
| 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:936 | brain disease | A central nervous system disease that is located_in the brain. |
| 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:3093 | nervous system cancer | An organ system cancer located_in the nervous system that affects the central or peripheral nervous system. |
| DOID:3620 | central nervous system cancer | A nervous system cancer that is located_in the central nervous system. |
| DOID:0050902 | medulloblastoma | An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. |
| DOID:1319 | brain cancer | A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. |
| DOID:4706 | infratentorial cancer | A brain cancer that is located_in the infratentorial region. |
| DOID:0080706 | medulloblastoma non-WNT/non-SHH | A medulloblastoma that is characterized as a molecular subtype that is not associated with activation of the WNT pathway or sonic hedgehog (SHH) pathway and TP53 mutations are absent. |
| DOID:0080708 | medulloblastoma non-WNT/non-SHH group 4 | A medulloblastoma non-WNT/non-SHH that is characterized as a molecular subtype by the absence of MYC amplifications and TP53 mutations, while chromosome 17 abnormalities may be present. |
14 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0080706 | DOID:0080708 |
| is_a | DOID:1319 | DOID:0080708 |
| is_a | DOID:4 | DOID:0080708 |
| is_a | DOID:863 | DOID:0080708 |
| is_a | DOID:14566 | DOID:0080708 |
| is_a | DOID:4706 | DOID:0080708 |
| is_a | DOID:331 | DOID:0080708 |
| is_a | DOID:7 | DOID:0080708 |
| is_a | DOID:3093 | DOID:0080708 |
| is_a | DOID:936 | DOID:0080708 |
| is_a | DOID:0050686 | DOID:0080708 |
| is_a | DOID:0050902 | DOID:0080708 |
| is_a | DOID:162 | DOID:0080708 |
| is_a | DOID:3620 | DOID:0080708 |
