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
05236 HMLR2 syndrome, Heimler, type 2 (HMLR2) 616617 AR 0 0 PEX6 - -
03758 PBD-4B peroxisome biogenesis disorder, type 4B (PBD-4B) 614863 - 2 2 PEX6 - -
03757 PBD4A peroxisome biogenesis disorder, type 4A (PBD4A, Zellweger) 614862 AR 1 1 PEX6 - -
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