All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06679 BANDDOS Brain abnormalities, neurodegeneration, and dysosteosclerosis 618476 AR - - CSF1R - -
01749 HDLS leukoencephalopathy, diffuse hereditary, with spheroid (HDLS) 221820 AD 3 1 CSF1R - -
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