All diseases

OMIM ID
606232
OMIM term:
CHROMOSOME 22q13.3 DELETION SYNDROME
Alternative terms:
TELOMERIC 22q13 MONOSOMY SYNDROME
PHELAN-MCDERMID SYNDROME
(∗) Location:
22q13.33  
(†) Associated OMIM genes:
SHANK3  
(‡) Associated MGI genes:

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