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Disease Ontology Browser
Griscelli syndrome type 3 (DOID:0060834)
Synonyms: Griscelli-Pruniras syndrome type 3; GS3
Alt IDs: OMIM:609227, ICD10CM:E70.3, MESH:C537303, ORDO:381, ORDO:79478, UMLS_CUI:C1836573
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.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/11/2017
MGI 6.08
The Jackson Laboratory