All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00002 JBTS-1 Joubert syndrome, type 1 (JBTS-1) 213300 - - - AHI1, CEP290, INPP5E, TCTN1, TMEM67 - -
00003 JBTS-13 Joubert syndrome, type 13 (JBTS-13) 614173 - - - TCTN1 - -
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