Leukoencephalopathy, diffuse hereditary, with spheroids 1
Also known as ALSP, Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia, CSF1R-related ALSP, CSF1R-related adult-onset leukoencephalopathy with axonal spheroids and pigmented glia+20 more
ALSP, Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia, CSF1R-related ALSP, CSF1R-related adult-onset leukoencephalopathy with axonal spheroids and pigmented glia, FPSG, GPSC, POLD, adult-onset leukoencephalopathy with axonal spheroids and pigmented glia, autosomal dominant leukoencephalopathy with neuroaxonal spheroids, dementia, familial, Neumann type, familial dementia, Neumann type, familial progressive subcortical gliosis, gliosis, familial progressive subcortical, leukoencephalopathy with neuroaxonal spheroids, autosomal dominant, leukoencephalopathy, adult-onset, with axonal spheroids and pigmented glia, pigmentary orthochromatic leukodystrophy, subcortical gliosis of Neumann, adult-onset leukodystrophy with neuroaxonal spheroids, hereditary diffuse leukoencephalopathy with axonal spheroids, neuroaxonal leukodystrophy, HDLS, hereditary diffuse leukoencephalopathy with spheroids, leukoencephalopathy, diffuse hereditary, with spheroids, leukoencephalopathy, hereditary diffuse, with spheroids.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
ALSP, Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia, CSF1R-related ALSP, CSF1R-related adult-onset leukoencephalopathy with axonal spheroids and pigmented glia, FPSG, GPSC, POLD, adult-onset leukoencephalopathy with axonal spheroids and pigmented glia, autosomal dominant leukoencephalopathy with neuroaxonal spheroids, dementia, familial, Neumann type, familial dementia, Neumann type, familial progressive subcortical gliosis, gliosis, familial progressive subcortical, leukoencephalopathy with neuroaxonal spheroids, autosomal dominant, leukoencephalopathy, adult-onset, with axonal spheroids and pigmented glia, pigmentary orthochromatic leukodystrophy, subcortical gliosis of Neumann, adult-onset leukodystrophy with neuroaxonal spheroids, hereditary diffuse leukoencephalopathy with axonal spheroids, neuroaxonal leukodystrophy, HDLS, hereditary diffuse leukoencephalopathy with spheroids, leukoencephalopathy, diffuse hereditary, with spheroids, leukoencephalopathy, hereditary diffuse, with spheroids
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.