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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:
Mouse
Zebrafish
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