All diseases

OMIM ID
208100
OMIM term:
ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE; AMCN
Alternative terms:

(∗) Location:
5q35  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
pma  

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* quick link - http://q.sanger.ac.uk/lkvg2kfe