Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease   1230303001

SNOMED CT code


SNOMED code1230303001
nameFatal congenital hypertrophic cardiomyopathy due to glycogen storage disease
statusactive
date introduced2022-06-30
fully specified name(s)Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease (disorder)
synonyms
  • Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease
  • Fatal congenital hypertrophic cardiomyopathy due to glycogenosis
attributes - group2
Due toGlycogen storage disease   29633007
attributes - group1
OccurrenceCongenital   255399007
Finding siteMyocardium structure   74281007
Associated morphologyHypertrophy   56246009
Pathological processPathological developmental process   308490002
parents
  • Autosomal dominant hereditary disorder   11164009
  • Congenital anomaly of myocardium   204394002
  • Glycogen storage disease   29633007
  • Cardiovascular system hereditary disorder   363005004
  • Developmental hereditary disorder   363070008
  • Hypertrophic cardiomyopathy due to glycogen storage disease   871638006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease   1230303001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Cardiac finding   301095005
        Myocardial finding   251052000
          Myocardial disease   57809008
            Congenital anomaly of myocardium   204394002
              Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease   1230303001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of carbohydrate metabolism   20957000
          Glycogen storage disease   29633007
            Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease   1230303001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        Cardiovascular system hereditary disorder   363005004
          Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease   1230303001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease   1230303001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Cardiac finding   301095005
        Heart disease   56265001
          Cardiac complication   40172005
            Cardiomyopathy due to storage disease   860839005
              Hypertrophic cardiomyopathy due to glycogen storage disease   871638006
                Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease   1230303001

ancestors
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