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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: Chédiak-Higashi-like syndrome, Chediak-Higashi-like syndrome, Griscelli-Pruniéras syndrome, Griscelli-Prunieras syndrome, partial albinism-immunodeficiency syndrome

Xenbase Genes : rab27a, mlph, myo5a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018306 - Griscelli syndrome


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)