Human genes for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia [DOID:0080523]
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.
Synonyms: adult-onset leukoencephalopathy with axonal spheroids and pigmented glia, adultonset leukoencephalopathy with axonal spheroids and pigmented glia, adult-onset leukoencephalopathy with axonal spheroids and pigmented glias, DOID:0080523, hereditary diffuse leukoencephalopathy with spheroids ...