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Disease Ontology Browser
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (DOID:0080523)
Alliance: disease page
Synonyms: hereditary diffuse leukoencephalopathy with spheroids
Alt IDs: OMIM:221820, ORDO:313808
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory