Rare nevus

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Rare nevus

ORPHA:294057Category

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

Genes reported in subtypes

ACTBAKT1ALKBRAFGJB2HRASKRASKRT13KRT4MMENEK9NRASNSDHLPIK3CAPTENRAF1SOX5ZEB2

Orphanet records these genes on 14 more specific entries under this disorder, not on this entry itself:

Becker nevus syndromeCHILD syndromeCLOVES syndromeCowden syndromeLarge/giant congenital melanocytic nevusLinear nevus sebaceus syndromeMME-related autosomal dominant Charcot Marie Tooth disease type 2Nevus comedonicus syndromePhakomatosis pigmentokeratoticaPorokeratotic eccrine ostial and dermal duct nevusProteus-like syndromeProteus syndromeSegmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndromeWhite sponge nevus

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

MONDO 17414UMLS C5680997

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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