All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00139 ID intellectual disability (ID) - - 2194 1893 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 540 more - -
03759 PBD5A peroxisome biogenesis disorder, type 5A (PBD-5A) 614866 AR 0 0 PEX2 - -
03760 PBD5B peroxisome biogenesis disorder, type 5B (PBD-5B) 614867 AR 0 0 PEX2 - -
03765 PBD7A peroxisome biogenesis disorder, type 7A (PBD-7A) 614872 AR 1 1 PEX26 - -
03766 PBD7B peroxisome biogenesis disorder, type 7B (PBD-7B) 614873 AR 2 2 PEX26 - -
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