All diseases

OMIM ID
613355
OMIM term:
CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME
Alternative terms:

(∗) Location:
17q23.1-q23.2  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/7bd2ooes