has material basis in germline mutation in CSF1R leukodystrophy leukoencephalopathy, hereditary diffuse, with spheroids CSF1R-related disorder leukoencephalopathy, diffuse hereditary, with spheroids 1 https://github.com/monarch-initiative/mondo/issues/7146 https://www.malacards.org/card/leukoencephalopathy_hereditary_diffuse_with_spheroids_1 leukoencephalopathy, hereditary diffuse, with spheroids MEDGEN:1794139 GARD:0010981 NORD:2033 SCTID:702427005 hereditary diffuse leukoencephalopathy with axonal spheroids MONDO:0800027 adult-onset leukoencephalopathy with axonal spheroids and pigmented glia ALSP dementia, familial, Neumann type hereditary diffuse leukoencephalopathy with spheroids leukoencephalopathy with neuroaxonal spheroids, autosomal dominant HDLS UMLS:C5561929 CSF1R-related ALSP OMIM:221820 GPSC adult-onset leukodystrophy with neuroaxonal spheroids pigmentary orthochromatic leukodystrophy Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia leukoencephalopathy, adult-onset, with axonal spheroids and pigmented glia autosomal dominant leukoencephalopathy with neuroaxonal spheroids FPSG NCIT:C153289 subcortical gliosis of Neumann familial dementia, Neumann type familial progressive subcortical gliosis Orphanet:313808 A rare autosomal dominant disease characterized by a complex phenotype including progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy. POLD DOID:0080523 leukoencephalopathy, diffuse hereditary, with spheroids neuroaxonal leukodystrophy gliosis, familial progressive subcortical CSF1R-related adult-onset leukoencephalopathy with axonal spheroids and pigmented glia ICD9:323.81 MESH:C580150