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
02735 CDG1H glycosylation, congenital disorder of, type Ih (CDG-1H) 608104 AR 2 - ALG8 - -
05719 PCLD3 liver disease, polycystic, type 3 (PCLD3) 617874 AD - - ALG8 - -
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