MPDU1-CDG - mannose-P-dolichol utilization defect 1 - congenital disorder of glycosylation (8749617)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT MPDU1-CDG - mannose-P-dolichol utilization defect 1 - congenital disorder of glycosylation
MAJOR CONCEPT File: 757, IEN: 7460948
DESIGNATION CODE
  • 3437621013
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH