All diseases

OMIM ID
235730
OMIM term:
MOWAT-WILSON SYNDROME
Alternative terms:
MICROCEPHALY, MENTAL RETARDATION, AND DISTINCT FACIAL FEATURES, WITH OR WITHOUT HIRSCHSPRUNG DISEASE
HIRSCHSPRUNG DISEASE-MENTAL RETARDATION SYNDROME
(∗) Location:
2q22.3  
(†) Associated OMIM genes:
ZEB2  
(‡) Associated MGI genes:
Zeb2  

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