MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation (8760254)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation
MAJOR CONCEPT File: 757, IEN: 7469443
DESIGNATION CODE
  • 3499449018
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH