Hematologic Malignancy
Pediatric and/or Germline Mutation-Associated Myeloid Disorders
CI-CAN-00001395Explore in graph →
- NCIt
- C198663
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Hematologic Malignancy
CI-CAN-00001395Explore in graph →
Data completeness3 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
A group of myeloid disorders that occur in childhood and/or are associated with germline gene mutations. It includes juvenile myelomonocytic leukemia, juvenile myelomonocytic leukemia-like neoplasm, refractory cytopenia of childhood, Noonan syndrome-associated myeloproliferative disorder, and myeloid neoplasm with germline predisposition.
Data updated 22 days agoSource updated 26.08e
Taxonomy
Several hierarchies coexist; edges are listed per hierarchy type with their source.
Parents
25 descendants in total; counters on this page aggregate over all of them.
Anatomy
Data updated 18 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 18 hours agoSource updated unknownregistry figures: none · counters aggregate over descendants