All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01278 CADASIL arteriopathy, cerebral, autosomal dominant, with subcortical infarcts and leukoencephalopathy (CADASIL) 125310 - 167 165 NOTCH3 - -
03889 IMF-2 myofibromatosis, infantile, type 2 (IMF-2) 615293 - 0 0 NOTCH3 - -
04331 LMNS meningocele, lateral syndrome (LMNS) 130720 - 0 0 NOTCH3 - -
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