All diseases

OMIM ID
610829
OMIM term:
HOLOPROSENCEPHALY 9; HPE9
Alternative terms:
PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES
HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES
(∗) Location:
2q14.2  
(†) Associated OMIM genes:
GLI2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/9ayemtnh