All diseases

OMIM ID
216360
OMIM term:
COACH SYNDROME
Alternative terms:
CEREBELLAR VERMIS HYPO/APLASIA, OLIGOPHRENIA, CONGENITAL ATAXIA, OCULAR COLOBOMA, AND HEPATIC FIBROSIS
JOUBERT SYNDROME WITH CONGENITAL HEPATIC FIBROSIS
(∗) Location:
16q12.2   4p15.32   8q22.1  
(†) Associated OMIM genes:
CC2D2A   RPGRIP1L   TMEM67  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/2snqudnk