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Griscelli syndrome type 3

MeSH: C537303ORPHA: 79478

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

Griscelli syndrome characterized by isolated silvery gray sheen of the hair and hypopigmentation of the skin that has material basis in mutation in the MLPH or MYO5A genes

Available Treatments (0)

No treatments linked yet

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

Clinical Presentation

Signs and symptoms associated with Griscelli syndrome type 3, sourced from HPO and Orphanet clinical annotations.

Hypopigmentation of hairPartial albinismIris hypopigmentation

Classification & Codes

MeSH Code

C537303

Orphanet Code

ORPHA:79478
Griscelli syndrome type 3
MeSHC537303
OrphanetORPHA:79478
Treatments0 drug(s)
Symptoms on record3 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO