All diseases

OMIM ID
611561
OMIM term:
MECKEL SYNDROME, TYPE 5; MKS5
Alternative terms:

(∗) Location:
16q12.2  
(†) Associated OMIM genes:
RPGRIP1L  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/1p5k9fcw