Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (8793771)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
MAJOR CONCEPT File: 757, IEN: 7482206
DESIGNATION CODE
  • 3638508016
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE MAJOR CONCEPT
SCOPE DIRECTLY LINKED
FORM MAJ