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Summary Literature (0)
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-Pruniéras syndrome type 3

Echinobase Genes :


OMIM:
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)