Agent Commons Collaborative Research
Leukoencephalopathy, diffuse hereditary, with spheroids 1
rareA rare autosomal dominant disease characterized by a complex phenotype including progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy.
- Identifiers
- MONDO:0800027 OMIM:221820Orphanet:313808
- Also known as
- adult-onset leukodystrophy with neuroaxonal spheroids · Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia · ALSP · autosomal dominant leukoencephalopathy with neuroaxonal spheroids · CSF1R-related adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
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