Glycogen storage disease, muscular form   15978003

SNOMED CT code


SNOMED code15978003
nameGlycogen storage disease, muscular form
statusactive
date introduced2002-01-31
fully specified name(s)Glycogen storage disease, muscular form (disorder)
synonymsGlycogen storage disease, muscular form
attributes - group2
Finding siteSkeletal muscle structure   127954009
attributes - group1
OccurrenceCongenital   255399007
parents
children
  • Equine polysaccharide storage myopathy   405730003  removed: 2014-01-31
  • Glycogen storage disease due to muscle beta-enolase deficiency   1162916008
  • Glycogen storage disease type III   66937008
  • Glycogen storage disease, type IV   11179002
  • Glycogen storage disease, type V   55912009
  • Glycogen storage disease, type VII   89597008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Muscle finding   106030000
      Disorder of muscle   129565002
        Disorder of skeletal muscle   75047002
          Metabolic myopathy   26111005
            Glycogen storage disease, muscular form   15978003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of carbohydrate metabolism   20957000
          Glycogen storage disease   29633007
            Glycogen storage disease, muscular form   15978003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Glycogen storage disease, muscular form   15978003

ancestors
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