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) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
00748 TTD trichothiodystrophy (TTD) - - - - ERCC2, ERCC3, GTF2H5, MPLKIP - -
04324 TTD-2 trichothiodystrophy, type 2, photosentitive (TTD-2) 616390 - - - ERCC3 - -
02968 XPB xeroderma pigmentosum, complementation group B (XPB) 610651 - - - ERCC3 - -
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