Subtype
Ependymoma with Genetic Abnormalities
CI-CAN-00007651Explore in graph →
Non-malignant17 evidence items
- NCIt
- C222261
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Subtype
CI-CAN-00007651Explore in graph →
Data completeness2 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
A term that refers to ependymomas associated with the presence of molecular and/or cytogenetic abnormalities. Representative examples include supratentorial ependymomas with ZFTA fusion or YAP1 fusion, spinal cord ependymomas with NF2 mutation, group A (PFA) or group B (PFB) posterior fossa ependymomas, and ependymomas with chromosomal losses and gains (e.g., 22q loss, 6q loss, 1q gain).
Data updated 22 days agoSource updated 26.08e
Taxonomy
Several hierarchies coexist; edges are listed per hierarchy type with their source.
Parents
9 descendants in total; counters on this page aggregate over all of them.
Anatomy
Data updated 19 hours agoSource updated unknowncounters aggregate over descendants
Names
Only the preferred name is recorded so far.
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Key figures
Each figure carries its unit, period and source; ranks link to "Why this rank?".
No registry-level ancestor: burden figures are published for the mutually exclusive top-level site groups only, and this entity does not descend from one. Global figures (IARC / GLOBOCAN) stay under license review and SEER awaits credentials.
Data updated 19 hours agoSource updated unknownregistry figures: none · counters aggregate over descendants