Adrenal/paraganglial tumor

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Adrenal/paraganglial tumor

ORPHA:100091Category

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Classified as
Category

Recorded for the broader condition

Prevalence
6-9 / 10 000 (Europe)Tumor of endocrine glands

Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.

Genes reported in subtypes

CCND1CDKN1BCDKN2ACDKN2BCLCN2CTNNB1MEN1PDE11APRKAR1ARETTERTTP53VHLZNRF3

Orphanet records these genes on 7 more specific entries under this disorder, not on this entry itself:

A well-studied disease is usually split into subtypes, and the gene is curated on whichever one the evidence belongs to. Open a subtype to see which gene goes with it.

Cross-references

GARD 19765UMLS C5681806

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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