DOID:0060834 - Griscelli syndrome type 3
Disease Ontology Definition: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.
Synonyms: GS3, Griscelli-PruniÃ©ras syndrome type 3
Echinobase Genes :
|OMIM:609227 - griscelli syndrome, type 3; gs3|
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Griscelli syndrome (is_a)