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
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 - -
00002 JBTS-1 Joubert syndrome, type 1 (JBTS-1) 213300 - - - AHI1, CEP290, INPP5E, TCTN1, TMEM67 - -
00920 JBTS-3 Joubert syndrome, type 3 (JBTS-3) 608629 - - - AHI1 - -
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