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
05109 JBTS Joubert syndrome (JBTS) - - 655 602 AHI1, ARL3, ARMC9, B9D1, CEP104, CEP290, MKS1, TCTN2, TMEM67 - -
06166 JBTS24 Joubert syndrome 24 616654 AR 1 1 TCTN2 - -
00707 MKS8 Meckel syndrome, type 8 (MKS-8) 613885 AR - - TCTN2 - -
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