All diseases

OMIM ID
164210
OMIM term:
HEMIFACIAL MICROSOMIA; HFM
Alternative terms:
OCULOAURICULOVERTEBRAL SPECTRUM; OAVS
GOLDENHAR SYNDROME
OCULOAURICULOVERTEBRAL DYSPLASIA
OAV DYSPLASIA
FACIOAURICULOVERTEBRAL SEQUENCE
FAV SEQUENCE
(∗) Location:
14q32  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Hfm   Zic3  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/8w9sdmxc