Hematologic Malignancy
Myelodysplastic Syndrome with TP53 Inactivation
CI-CAN-00006076Explore in graph →
Hematologic
- NCIt
- C200377
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Hematologic Malignancy
CI-CAN-00006076Explore in graph →
Data completeness0 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
Myelodysplastic syndrome characterized by the presence of TP53 gene inactivating alterations. They include monoallelic or biallelic TP53 gene mutations or one TP53 gene mutation and concurrent copy loss of TP53.
Data updated 22 days agoSource updated 26.08e
Taxonomy
Several hierarchies coexist; edges are listed per hierarchy type with their source.
Parents
Children (2)
4 descendants in total; counters on this page aggregate over all of them.
Anatomy
Data updated 11 hours agoSource updated unknowncounters aggregate over descendants
Names
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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 11 hours agoSource updated unknownregistry figures: none · counters aggregate over descendants