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Extrarenal Rhabdoid Tumor · CancerIndex

Cancers
Neoplasm
Neoplasm by Special Category
Malignant Neoplasm
Childhood Malignant Neoplasm
Extrarenal Rhabdoid Tumor

Subtype

Extrarenal Rhabdoid Tumor

CI-CAN-00000864Explore in graph →

Pediatric

NCIt: C6586

Overview
Statistics
Survival
Genomics
Variants & evidence
Drugs
Trials1
Research
Rankings
Sources & provenance

Data completeness2 / 7 dimensions

Epidemiology (no data yet)
Survival (no data yet)
Trials (data present)
Literature (data present)
Genomics (no data yet)
Evidence (no data yet)
Therapies (no data yet)

Computed from entity_counters.completeness · refreshed after each connector run

Definition

What this entity is

A rhabdoid tumor which arises in the soft tissues. It occurs in infants and children and may be associated with loss of chromosome 22. It is characterized by the presence of cells with a large eccentric nucleus, prominent nucleolus, and abundant cytoplasm.

Definition text as published by ncit-evsProvenance

Source: NCI Thesaurus (NCIt)
Dataset: NCI Thesaurus
Version: 26.08e
Retrieved: Sep 8, 2026
Layer: raw (as published)
Evidence: expert curation
License: CC BY 4.0
Run: ING-NCITEVS-20260908-000001

Open at source Curated

Data updated 22 days agoSource updated 26.08e

Taxonomy

Position in the hierarchies

Several hierarchies coexist; edges are listed per hierarchy type with their source.

Parents

ncit

Childhood Connective and Soft Tissue NeoplasmCancer Family
Childhood Malignant NeoplasmCancer Family
Malignant Soft Tissue Neoplasm of Uncertain DifferentiationSubtype
Rhabdoid TumorCancer Family

Children (3)

ncit

Extrarenal Rhabdoid Tumor of the Liver
Extrarenal Rhabdoid Tumor of the Ovary
Extrarenal Rhabdoid Tumor of the Prostate

Anatomy

Anatomical sites

Connective and Soft TissueC3810

Record

Identity

CancerIndex ID: CI-CAN-00000864
Entity type: Subtype
Malignant: Yes
Solid / hematologic: Solid tumor
Pediatric relevant: Yes
Rare cancer: Unknown (no incidence data yet)
Hierarchy depth: 4
Classification version: 26.08e
Semantic types: Neoplastic Process
Status: Active
Record updated: 2026-09-08

Coverage

Data completeness

Trials (all / active): 1 / 0

Publications (all / 5y)

83 / 18

Evidence items

0

Genes / variants

0 / 0

Drugs (any / approved)

0 / 0

Genomic cohorts

0

Epidemiology / survival obs.

0 / 0

Data updated 9 hours agoSource updated unknowncounters aggregate over descendants

Names

Synonyms (2)

Malignant Extrarenal Rhabdoid Neoplasmsynonym · NCIt
Rhabdoid Tumor of Soft Tissuesynonym · NCIt

CancerIndex is a research and information platform. It does not diagnose and does not recommend treatment.

Key figures

At a glance

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.

Active trials0countcurrent registry status · entity + descendantsclinicaltrialsComputednot in a current ranking snapshot
Recruiting trials0countstatus RECRUITING · entity + descendantsclinicaltrialsComputednot in a current ranking snapshot
Curated evidence items0countaccepted CIViC items · entity + descendantscivicComputednot in a current ranking snapshot
Publications, last 12 months1countPubMed records · stored query · 12-month windowpubmedComputedrank #1866 of 2,294 (World · both sexes · all ages · latest · all malignant entities)
Genomic cohorts0countopen GDC projects · entity + descendantsgdcComputednot in a current ranking snapshot

Data updated 9 hours agoSource updated unknownregistry figures: none · counters aggregate over descendants