Griscelli syndrome type 3

MONDO:0012220

A 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.

Also known as: GS3, Griscelli syndrome type 3, Griscelli-PruniC)ras syndrome type 3, Griscelli-Pruniéras syndrome type 3, Griscelli-Pruni��ras syndrome type 3, Griscelli disease type 3, Griscelli syndrome, type 3, hypomelanosis with no immunologic or neurologic manifestations

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