Subtype
Central Nervous System Hemangioblastoma
CI-CAN-00002139Explore in graph →
Non-malignant1 active trials
- NCIt
- C7007
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Subtype
CI-CAN-00002139Explore in graph →
Data completeness1 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
A rare, highly vascular, WHO grade I tumor that arises from the central nervous system and is composed of abundant capillaries and stromal cells. It can occur sporadically or as part of von Hippel-Lindau syndrome. It is a slow growing tumor with a low risk of metastasis, despite its benign histological features.
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 3 hours agoSource updated unknowncounters aggregate over descendants
Names
CancerIndex is a research and information platform. It does not diagnose and does not recommend treatment.
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 3 hours agoSource updated unknownregistry figures: none · counters aggregate over descendants