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Ontology Browser

Term:
Griscelli syndrome type 3 (DOID:0060834)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
Griscelli syndrome +     
Griscelli syndrome type 1  
Griscelli syndrome type 2  
Griscelli syndrome type 3  
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 Synonyms: GS3 ;   Griscelli-Prunieras syndrome type 3 ;   Griscelli-PruniĆ©ras syndrome type 3 ;   Hypomelanosis with no immunologic or neurologic manifestations
Primary IDs: MESH:C537303
Alternate IDs: OMIM:609227
Xrefs: GARD:9715 ;   ORDO:79478
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/12148598 "DO", https://www.ncbi.nlm.nih.gov/pubmed/12897212 "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.