All diseases

OMIM ID
612285
OMIM term:
JOUBERT SYNDROME 9; JBTS9 JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED
Alternative terms:

(∗) Location:
4p15.32  
(†) Associated OMIM genes:
CC2D2A  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/uu6g4rau