Autosomal recessive muscular dystrophy due to LAP1B (lamin-associated protein 1B) deficiency (8751938)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive muscular dystrophy due to LAP1B (lamin-associated protein 1B) deficiency
MAJOR CONCEPT File: 757, IEN: 7462356
DESIGNATION CODE
  • 3446317017
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH