raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:276624

OBSOLETE: Sporadic pheochromocytoma

inactive · referred to ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Sporadic pheochromocytoma/secreting paraganglioma

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Sporadic pheochromocytoma
frOBSOLETE : Phéochromocytome sporadique
deOBSOLET: Phaeochromozytom, sporadisches
esOBSOLETO: Feocromocitoma esporádico
itOBSOLETO: Feocromocitoma sporadico
nlOBSOLEET: Sporadisch feochromocytoom
ptOBSOLETO: Feocromocitoma esporádico
plNIEAKTUALNE: Guz chromochlonny sporadyczny
csNEAKTUÁLNÍ: Sporadický feochromocytom
ukСпорадична феохромоцитома
zh弃用:散发性嗜铬细胞瘤
trEski adı: Sporadik feokromositom
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card