Molecular Subtype
MYOD1-Mutant Spindle Cell/Sclerosing Rhabdomyosarcoma
CI-CAN-00008084Explore in graph →
- NCIt
- C178235
Loading cancer entity…
Molecular Subtype
CI-CAN-00008084Explore in graph →
Data completeness0 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
Spindle cell/sclerosing rhabdomyosarcoma characterized by the presence of MYOD1 p.Leu122Arg substitution mutation. This subtype includes most spindle cell/sclerosing rhabdomyosarcomas in adolescents and young adults, as well as some cases in older adults. It follows 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.
Parents
Children (0)
Leaf node — no children.
Anatomy
Data updated 14 hours agoSource updated unknowncounters aggregate over descendants
Names
Only the preferred name is recorded so far.
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 14 hours agoSource updated unknownregistry figures: none · counters aggregate over descendants