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
02907 ARMD7 macular degeneration, age-related, type 7 (ARMD-7) 610149 - - - HTRA1 - -
06072 CADASIL2 Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 616779 AD 1 1 HTRA1 - -
02291 CARASIL CARASIL syndrome 600142 AR - - HTRA1 - -
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