Syndromic microphthalmia due to OTX2 mutation (8696122)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Syndromic microphthalmia due to OTX2 mutation
MAJOR CONCEPT File: 757, IEN: 7454731
DESIGNATION CODE
  • 3313769012
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH