All diseases

OMIM ID
610828
OMIM term:
HOLOPROSENCEPHALY 7; HPE7
Alternative terms:

(∗) Location:
9q22.32  
(†) Associated OMIM genes:
PTCH1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/hi51rslm