adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

Summary

DOID:0080523 - adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

Disease Ontology 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.

Synonyms: hereditary diffuse leukoencephalopathy with spheroids,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), leukodystrophy (is_a)