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Publication

Sporadic phaeochromocytoma in childhood: clinical and molecular variability.

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J Pediatr Endocrinol Metab2005PMID 16042317stubpubmedProvenance
Source
PubMed
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-CIVIC-20260908-000001
Published

Abstract

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Linked entities

Linked entities (2)

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Validated 2

Curated evidence

Evidence citing this paper (1)

civicProvenance
Source
CIViC — Clinical Interpretation of Variants in Cancer
Dataset
CIViC evidence items
Version
civic-2026-09-08
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Evidence
expert curation
License
CC0 1.0
PMID
16042317
Run
ING-CIVIC-20260908-000001
Open at source
CuratedShowing 1–1 of 1 evidence items · levels, directions and significance as curated at the source; each row links to its CIViC record.
TherapyCancerTypeLevelDirection · significanceRating (1–5)StatusEvidenceSource
VHL R167W (c.499C>T)1
(predisposing)Von Hippel-Lindau DiseaseUNRESOLVEDPredisposingCSupports Predisposition3accepted
EID8469

A 10.5 year old male patient was diagnosed with adrenal pheochromocytoma. He had intermittent abdominal pain for 6 months. A CT scan showed a left adrenal solid tumor (3x3cm) with no calcifications an… (full text at CIViC)

PMID 16042317 · Pozo et al., 2005 · Open in CIViC

civic