Griscelli syndrome type 2

Summary
Synonym
  • GS2
  • Griscelli syndrome with hemophagocytic syndrome
  • Griscelli-Prunieras syndrome type 2
  • PAID syndrome
  • hypopigmentation-immunodeficiency with or without neurologic impairment syndrome
  • partial albinism and immunodeficiency syndrome
Definition
A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and immunodeficiency with or without neurologic impairment that has_material_basis_in mutation in the RAB27A gene on chromosome 15q21.3.
Super Class
Griscelli syndrome
External Links
Disease Ontology
DOID:0060833
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
2752 GLUL glutamate-ammonia ligase
3423 IDS iduronate 2-sulfatase
Related Glycoprotein
Displaying all 2 entries
UniProt ID Protein Name Source
P15104 Glutamine synthetase
P22304 Iduronate 2-sulfatase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024