Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder) (8793772)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder)
MAJOR CONCEPT File: 757, IEN: 7482206
DESIGNATION CODE
  • 3638507014
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE FULLY SPECIFIED NAME
SCOPE DIRECTLY LINKED
FORM FSN