All diseases

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00024 CADASIL Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy - - 6 5 NOTCH3 - -
00025 OTCD Ornithine transcarbamylase deficiency - - 2 2 OTC - -
Legend   How to query