Autosomal dominant hereditary disorder
Cardiovascular system hereditary disorder
Glycogen storage disease
Hypertrophic cardiomyopathy due to glycogen storage disease
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Protein kinase adenosine monophosphate-activated non catalytic subunit gamma 2 syndrome (disorder)
PRKAG2 syndrome
Protein kinase adenosine monophosphate-activated non catalytic subunit gamma 2 syndrome
Id358501000112100
StatusPrimitive
Due toGlycogen storage disease
OccurrenceCongenital
Associated morphologyHypertrophy
Finding siteMyocardium structure
SNOMED CT to ICD-10 extended map
TargetE74.0
RuleTRUE
AdviceALWAYS E74.0
CorrelationSNOMED CT source code to target map code correlation not specified
TargetI43.1
RuleTRUE
AdviceALWAYS I43.1 | THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
CorrelationSNOMED CT source code to target map code correlation not specified