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
01559 SNDNS Sneddon syndrome (livedo reticularis and cerebrovascular accidents) 182410 AR - - CECR1 - -
04401 VAIHS Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome 615688 AR - - CECR1 - -
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