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
00018 - 17-beta-hydroxysteroid dehydrogenase X deficiency 300438 - - - HSD17B10 - -
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 - -
00019 MRX-17;MRX-31 mental retardation, X-linked, type 17/31 (MRX-17;MRX-31, chromosome Xp11.22 duplication syndrome) 300705 - - - HSD17B10 - -
00017 MRXS-10 mental retardation, X-linked syndromic, type 10 (MRXS-10) 300220 - - - HSD17B10 - -
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