All diseases

OMIM ID
266265
OMIM term:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C
Alternative terms:
CDG IIc; CDGIIc
LEUKOCYTE ADHESION DEFICIENCY, TYPE II; LAD2
RAMBAM-HASHARON SYNDROME; RHS
(∗) Location:
11p11.2  
(†) Associated OMIM genes:
SLC35C1  
(‡) Associated MGI genes:
Slc35c1  

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