All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00139 ID intellectual disability (ID) - - 1413 1151 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 527 more - -
01703 PBD2A peroxisome biogenesis disorder, type 2A (PBD2A) 214110 AR 0 0 PEX5 - -
01634 PBD2B peroxisome biogenesis disorder, type 2B (PBD2B) 202370 AR 0 0 PEX5 - -
05829 RCDP5 chondrodysplasia punctata, rhizomelic, type 5 (RCDP5) 616716 AR 0 0 PEX5 - -
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