adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

Summary
Synonym
  • hereditary diffuse leukoencephalopathy with spheroids
Definition
A leukodystrophy that is characterized by progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy and has_material_basis_in heterozygous mutation in the CSF1R gene on chromosome 5q32.
Super Class
autosomal dominant disease leukodystrophy
External Links
Disease Ontology
DOID:0080523
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5476 CTSA cathepsin A
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P10619 Lysosomal protective protein

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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