All diseases

OMIM ID
216550
OMIM term:
COHEN SYNDROME; COH1
Alternative terms:
HYPOTONIA, OBESITY, AND PROMINENT INCISORS
PEPPER SYNDROME
CHS1, FORMERLY
(∗) Location:
8q22.2  
(†) Associated OMIM genes:
VPS13B  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/0b762tek