All diseases

OMIM ID
156200
OMIM term:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1 CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED
Alternative terms:

(∗) Location:
2q23.1  
(†) Associated OMIM genes:
MBD5  
(‡) Associated MGI genes:

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