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DOID:0060831 - Griscelli syndrome
Disease Ontology Definition:An autosomal recessive disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin.
Synonyms: Chédiak-Higashi-like syndrome, Griscelli-Pruniéras syndrome, partial albinism-immunodeficiency syndrome,
Echinobase Genes
:
rab27a
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a)