OBO ID: DOID:0060834
Term Name: Griscelli syndrome type 3 Search Ontology:
Synonyms: Griscelli-PruniƩras syndrome type 3, GS3
Definition: 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. (2)
References: ICD10CM:E70.3, MESH:C537303, OMIM:609227 (all 5) expand
Ontology: Human Disease   (DOID:0060834)
Relationships
is a type of:
OTHER Griscelli syndrome type 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MLPH mlphb, mlpha Griscelli syndrome, type 3 609227
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None