All diseases

OMIM ID
300673
OMIM term:
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
Alternative terms:

(∗) Location:
Xq28  
(†) Associated OMIM genes:
MECP2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/tne8s9fl