Term Name: adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
Synonyms: 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.
Ontology: Human Disease [DOID:0080523]   ( DOID:0080523 )

Relationships
is a type of: autosomal dominant disease leukodystrophy