All diseases

OMIM ID
257320
OMIM term:
LISSENCEPHALY 2; LIS2
Alternative terms:
LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE
NORMAN-ROBERTS SYNDROME
(∗) Location:
7q22.1  
(†) Associated OMIM genes:
RELN  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/tn55p3kl