All diseases

OMIM ID
608636
OMIM term:
CHROMOSOME 15q11-q13 DUPLICATION SYNDROME
Alternative terms:
DUPLICATION 15q11-q13 SYNDROME AUTISM, SUSCEPTIBILITY TO, 4, INCLUDED; AUTS4, INCLUDED
CHROMOSOME 15q11.2 MICRODUPLICATION SYNDROME, INCLUDED
(∗) Location:
15q11  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Dp(7Herc2-Mkrn3)1Taku  

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