Subtype
Hereditary Leiomyomatosis and Renal Cell Carcinoma
CI-CAN-00005495HLRCCExplore in graph →
- NCIt
- C51302
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Subtype
CI-CAN-00005495HLRCCExplore in graph →
Data completeness2 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
An autosomal dominant inherited syndrome caused by germline mutations in the FH gene. It is characterized by predisposition to renal cell carcinoma, leiomyomas of the skin and uterus, and leiomyosarcoma of the uterus.
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 19 hours agoSource updated unknowncounters aggregate over descendants
Names
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Key figures
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Data updated 19 hours agoSource updated unknownregistry figures: cdc-uscs · latest year available per metric · counters aggregate over descendants