All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01643 - aciduria, alpha-methylacetoacetic 203750 AR - - ACAT1 - -
01892 - deficiency, lecithin:cholesterol acyltransferase (Norum disease) 245900 AR - - LCAT - -
03533 ACAT2D acetyl-CoA acetyltransferase-2 deficiency (ACAT2D) 614055 IC - - ACAT2 - -
03547 ACATALASIA acatalasemia 614097 - - - CAT - -
01334 FED disease, fish-eye (FED) 136120 AR 4 1 LCAT - -
06449 HVLI ?Hypervalinemia or hyperleucine-isoleucinemia 618850 AR - - BCAT2 - -
03223 SPGF7 spermatogenic failure, type 7 (SPGF-7) 612997 AR - - CATSPER1 - -
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