Lissencephaly type 1 due to doublecortin gene mutation (8665719)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Lissencephaly type 1 due to doublecortin gene mutation
MAJOR CONCEPT File: 757, IEN: 7451468
DESIGNATION CODE
  • 3303690019
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH