SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Metabolic disease  75934005

Disorder of carbohydrate metabolism  20957000

Glycogen storage disease  29633007

Glycogen storage disease due to acid maltase deficiency  274864009

Glycogen storage disease due to acid maltase deficiency, late-onset   722343009

SNOMED CT code


SNOMED code722343009
nameGlycogen storage disease due to acid maltase deficiency, late-onset
statusactive
date introduced2017-01-31
fully specified name(s)Glycogen storage disease due to acid maltase deficiency, late-onset (disorder)
synonyms
  • Glycogen storage disease type II late onset
  • Glycogen storage disease due to acid maltase deficiency, late-onset
  • Alpha-1,4-glucosidase acid deficiency, late onset
  • Glycogenosis type II, late onset
  • Pompe disease, late onset
attributes - group2
Due toDeficiency of glucan 1,4-alpha-glucosidase   124454007
attributes - group1
OccurrenceCongenital   255399007
parentsGlycogen storage disease due to acid maltase deficiency   274864009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of carbohydrate metabolism   20957000
          Glycogen storage disease   29633007
            Glycogen storage disease due to acid maltase deficiency   274864009
              Glycogen storage disease due to acid maltase deficiency, late-onset   722343009

ancestors
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