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3MC syndrome 2

MeSH: C535586ORPHA: 2998

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

3MC syndrome that has material basis in homozygous mutation in the COLEC11 gene on chromosome 2p25

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

C535586

Orphanet Code

ORPHA:2998
3MC syndrome 2
MeSHC535586
OrphanetORPHA:2998
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO