All diseases

OMIM ID
603546
OMIM term:
SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY TYPE 2; SEMDJL2
Alternative terms:
SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, HALL TYPE
SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, LEPTODACTYLIC TYPE
SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH MULTIPLE DISLOCATIONS, HALL TYPE
(∗) Location:
16p11.2  
(†) Associated OMIM genes:
KIF22  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/drghm3tt