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
01892 - deficiency, lecithin:cholesterol acyltransferase (Norum disease) 245900 AR - - LCAT - -
01334 FED disease, fish-eye (FED) 136120 AR 4 1 LCAT - -
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