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 JBTS1 syndrome, Joubert, type 1 (JBTS1) 213300 AR 49 53 INPP5E, TCTN1, TMEM67 - -
00003 JBTS13 syndrome, Joubert, type 13 (JBTS13) 614173 AR 1 0 TCTN1 - -
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