Gerstmann-Straussler-Scheinker syndrome

Summary
Synonym
  • Gerstmann-Straussler-Scheinker disease
  • PRION DEMENTIA
Definition
A prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain.
Super Class
prion disease
External Links
Disease Ontology
DOID:4249
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 14 of 14 in total
Gene ID Gene Symbol Description Source
5836 PYGL glycogen phosphorylase L
5837 PYGM glycogen phosphorylase, muscle associated
6476 SI sucrase-isomaltase
8972 MGAM maltase-glucoamylase
The Human Phenotype Ontology
Displaying entries 31 - 38 of 38 in total
HPO ID HPO Term
HP:0000718 Aggressive behavior
HP:0003581 Adult onset
HP:0002063 Rigidity
HP:0001347 Hyperreflexia
HP:0000751 Personality changes
HP:0002186 Apraxia
HP:0000712 Emotional lability
HP:0002067 Bradykinesia
Displaying 1 entry
Gene ID Gene Symbol Description
5621 PRNP prion protein (Kanno blood group)

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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