Griscelli syndrome, type 2

Disease ID:1186
Name:Griscelli syndrome, type 2
Associated with:1 targets
0 immuno-relevant targets
0 immuno-relevant ligands
Description
Hypomelanosis with immunologic abnormalities with or without neurologic impairment, is caused by mutation in the RAB27A gene (MIM 603868).
Database Links
OMIM: 607624

Targets

Ligands

No ligand related data available for Griscelli syndrome, type 2