- OMIM ID
-
221820
- OMIM term:
- LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS
- Alternative terms:
-
LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT
GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC
DEMENTIA, FAMILIAL, NEUMANN TYPE
SUBCORTICAL GLIOSIS OF NEUMANN
- (∗) Location:
- 17q21-q22 5q32
- (†) Associated OMIM genes:
- CSF1R
- (‡) Associated MGI genes:
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