All diseases

OMIM ID
200990
OMIM term:
ACROCALLOSAL SYNDROME; ACLS
Alternative terms:
HALLUX DUPLICATION, POSTAXIAL POLYDACTYLY, AND ABSENCE OF CORPUS CALLOSUM
SCHINZEL ACROCALLOSAL SYNDROME JOUBERT SYNDROME 12, INCLUDED; JBTS12, INCLUDED
JOUBERT SYNDROME 12/15, DIGENIC, INCLUDED
(∗) Location:
15q26.1  
(†) Associated OMIM genes:
KIF7  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

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