Congenital disorder of glycosylation type II due to MAN1B1 deficiency (8760255)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Congenital disorder of glycosylation type II due to MAN1B1 deficiency
MAJOR CONCEPT File: 757, IEN: 7469443
DESIGNATION CODE
  • 3499451019
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH