| Disease Aliases (28) | Alsp Adult-onset leukodystrophy with neuroaxonal spheroids Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia Autosomal dominant leukoencephalopathy with neuroaxonal spheroids Csf1r-related hereditary diffuse leukoencephalopathy with spheroids Dementia, familial, neumann type Fpsg Familial dementia Familial dementia, neumann type Familial progressive subcortical gliosis Gliosis, familial progressive subcortical Gpsc Hdls Hdls - hereditary diffuse leukoencephalopathy with spheroids Hereditary diffuse leukoencephalopathy with axonal spheroids Hereditary diffuse leukoencephalopathy with spheroids Leukoencephalopathy with neuroaxonal spheroids, autosomal dominant Leukoencephalopathy, adult-onset, with axonal spheroids and pigmented glia Leukoencephalopathy, diffuse hereditary, with spheroids Neumann type Neuroaxonal leukodystrophy Pold Pigmentary orthochromatic leukodystrophy Subcortical gliosis of neumann Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia Leukoencephalopathy, diffuse hereditary, with spheroids; hdls Leukoencephalopathy, hereditary diffuse, with spheroids Leukoencephalopathy, hereditary diffuse, with spheroids; hdls |
Associated Genes (2) NCBI-RefSeq: AARS2 (Alanyl-tRNA synthetase 2, mitochondrial) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: CSF1R (Colony stimulating factor 1 receptor) External Links: gnomAD browser Ensembl GeneCards
| |||||||
| Cross-references of Hereditary diffuse leukoencephalopathy with spheroids | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |