RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
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. (DO)
Synonyms:
exact_synonym:
GS3; Griscelli-Prunieras syndrome type 3; Griscelli-Pruniéras syndrome type 3; Hypomelanosis with no immunologic or neurologic manifestations; MLPH-RELATED CONDITION