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Disease Ontology Browser
Griscelli syndrome (DOID:0060831)
Alliance: disease page
Synonyms: Chdiak-Higashi-like syndrome; Griscelli-Pruniras syndrome; partial albinism-immunodeficiency syndrome
Alt IDs: ICD10CM:E70.3, OMIM:PS214450, ORDO:381
Definition: An autosomal recessive disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin.

Disease References using Mouse Models (3)

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
02/11/2020
MGI 6.14
The Jackson Laboratory