Syndromic microphthalmia due to orthodenticle homeobox 2 mutation (disorder) (8680073) EXPRESSIONS (757.01)
Name
Value
DISPLAYABLE TEXT
Syndromic microphthalmia due to orthodenticle homeobox 2 mutation (disorder)
MAJOR CONCEPT
File: 757, IEN: 7454731
DESIGNATION CODE
3313766017
CODING SYSTEM:
SCT
HIERARCHY:
Disorder
TYPE
FULLY SPECIFIED NAME
SCOPE
DIRECTLY LINKED
FORM
FSN