Griscelli syndrome

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Summary

Literature (0)

DOID:0060831 - Griscelli syndrome

Disease Ontology Definition:An integumentary system disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin.

Synonyms: ChÃ©diak-Higashi-like syndrome, Griscelli-PruniÃ©ras syndrome, partial albinism-immunodeficiency syndrome, Chediak-Higashi-like syndrome, Griscelli-Prunieras syndrome

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: rab27a

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), integumentary system disease (is_a)