All diseases

OMIM ID
608443
OMIM term:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3
Alternative terms:

(∗) Location:
19p13.12  
(†) Associated OMIM genes:
CC2D1A  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/8p8bmwbe