Autosomal recessive cerebelloparenchymal disorder type 3 (8665151)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive cerebelloparenchymal disorder type 3
MAJOR CONCEPT File: 757, IEN: 7451128
DESIGNATION CODE
  • 3302379011
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH