All diseases

OMIM ID
610443
OMIM term:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17; MRD17
Alternative terms:
CHROMOSOME 17q21.31 DELETION SYNDROME
MICRODELETION 17q21.31 SYNDROME
(∗) Location:
17q21.31  
(†) Associated OMIM genes:
KANSL1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/fwip99ta