All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01749 HDLS leukoencephalopathy, diffuse hereditary, with spheroid (HDLS) 221820 2 0 CSF1R - -