All diseases

OMIM ID
132450
OMIM term:
EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS
Alternative terms:

(∗) Location:
12q13.11  
(†) Associated OMIM genes:
COL2A1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/5j08xgap