Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder) (8707456)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder)
MAJOR CONCEPT File: 757, IEN: 7461936
DESIGNATION CODE
  • 3442311019
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE FULLY SPECIFIED NAME
SCOPE DIRECTLY LINKED
FORM FSN