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Disease Ontology Browser
Griscelli syndrome type 3 (DOID:0060834)
Alliance: disease page
Synonyms: Griscelli-Pruniras syndrome type 3; GS3
Alt IDs: OMIM:609227, MESH:C537303, 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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
12/03/2019
MGI 6.14
The Jackson Laboratory