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

Glycogen storage disease, type V   55912009

SNOMED CT code


SNOMED code55912009
nameGlycogen storage disease, type V
statusactive
date introduced2002-01-31
fully specified name(s)Glycogen storage disease, type V (disorder)
synonyms
  • Glycogen storage disease type 5
  • Glycogenosis, type 5
  • McArdle disease
  • Glycogen storage disease type V
  • Glycogen storage disease, type V
  • Myophosphorylase deficiency glycogenosis
  • McArdle's disease
  • GSD V
  • Muscle glycogen phosphorylase deficiency
attributes - group2
Finding siteSkeletal muscle structure   127954009
attributes - group1
OccurrenceCongenital   255399007
parentsGlycogen storage disease, muscular form   15978003
hierarchies
a selection of possible paths
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
            Glycogen storage disease, type V   55912009

ancestors
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