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
05109 JBTS Joubert syndrome (JBTS) - - 647 593 AHI1, ARL3, ARMC9, B9D1, C5orf42, CEP104, CEP290, CSPP1, MKS1, TCTN2, TMEM67 - -
04039 JBTS21 Joubert syndrome, type 21 (JBTS-21) 615636 AR 2 2 CSPP1 - -
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