All diseases

OMIM ID
105830
OMIM term:
ANGELMAN SYNDROME; AS
Alternative terms:

(∗) Location:
15q11.2   Xp22.13   Xq28  
(†) Associated OMIM genes:
CDKL5   MECP2   UBE3A  
(‡) Associated MGI genes:
Snrpn   Ube3a  

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* quick link - http://q.sanger.ac.uk/behcijm0