All diseases

OMIM ID
607078
OMIM term:
EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5
Alternative terms:
MULTIPLE EPIPHYSEAL DYSPLASIA, MATN3-RELATED
MICROEPIPHYSEAL DYSPLASIA, BILATERAL HEREDITARY; BHMED
(∗) Location:
2p24.1  
(†) Associated OMIM genes:
MATN3  
(‡) Associated MGI genes:
Matn3  

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* quick link - http://q.sanger.ac.uk/17k0lf60