Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (8751301)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
MAJOR CONCEPT File: 757, IEN: 7461936
DESIGNATION CODE
  • 3442316012
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH