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Data completeness3 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
A rare poorly differentiated carcinoma characterized by rearrangement of the NUTM1 gene and the presence of balanced translocation t(15;19) that results in the creation of a fusion gene involving the NUTM1 gene, most commonly BRD4-NUTM1 fusion gene. It arises from midline epithelial structures, most commonly the head, neck, and mediastinum, and has an aggressive clinical course.
Data updated 22 days agoSource updated 26.08e
Taxonomy
Several hierarchies coexist; edges are listed per hierarchy type with their source.
Children (4)
8 descendants in total; counters on this page aggregate over all of them.
Anatomy
Data not yet available
Data updated 1 hour 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 1 hour agoSource updated unknownregistry figures: none · counters aggregate over descendants