SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Disorder of lysosomal enzyme  23585005

Lipid storage disease  10741005

Lipid storage myopathy   240095001

SNOMED CT code


SNOMED code240095001
nameLipid storage myopathy
statusactive
date introduced2002-01-31
fully specified name(s)Lipid storage myopathy (disorder)
synonymsLipid storage myopathy
attributes - group2
Finding siteSkeletal muscle structure   127954009
attributes - group1
OccurrenceCongenital   255399007
parents
children
  • Autosomal dominant myoglobinuria   725903003
  • Genetic recurrent myoglobinuria   716721003
  • Neutral lipid storage disease with myopathy   699315005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Disorder of lysosomal enzyme   23585005
          Lipid storage disease   10741005
            Lipid storage myopathy   240095001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Muscle finding   106030000
      Disorder of muscle   129565002
        Disorder of skeletal muscle   75047002
          Metabolic myopathy   26111005
            Lipid storage myopathy   240095001

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
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