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 AD 172 170 NOTCH3 - -
03889 IMF2 myofibromatosis, infantile, type 2 (IMF-2) 615293 AD - - NOTCH3 - -
04331 LMNS meningocele, lateral syndrome (LMNS) 130720 AD - - NOTCH3 - -
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