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Human Disease and Mouse Model Detail
Human Disease Leukoencephalopathy, Diffuse Hereditary, with Spheroids; HDLS
OMIM ID: 221820
Synonyms Dementia, Familial, Neumann Type; Gliosis, Familial Progressive Subcortical; GPSC; Leukoencephalopathy with Neuroaxonal Spheroids, Autosomal Dominant; Subcortical Gliosis of Neumann
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Csf1r CSF1R*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/18/2014
MGI 5.20
The Jackson Laboratory