Autosomal recessive hereditary disorder
Glycogen storage disease, hepatic form
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Glycogen storage disease, type VI (disorder)
Glycogen storage disease, type VI
Hers disease
Hepatic glycogen phosphorylase deficiency
GSD VI
Hepatic phosphorylase deficiency
glycogeenstapelingsziekte type 6
Id29291001
StatusPrimitive
OccurrenceCongenital
Finding siteLiver structure
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetE74.0
RuleTRUE
AdviceALWAYS E74.0
CorrelationSNOMED CT source code to target map code correlation not specified
TargetK77.8
RuleTRUE
AdviceALWAYS K77.8 | 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