fosforylase-b-kinasedeficiëntie
X-gebonden hereditaire recessieve aandoening
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Glycogen storage disease IXa1 (disorder)
Glycogen storage disease IXa1
XLG1 - X-linked liver glycogenosis type 1
PHKA2 gene related hepatic phosphorylase kinase alpha 2 subunit deficiency
GSD9A1 - glycogen storage disease type 9A1
Id1411498003
StatusPrimitive
Finding sitestructuur van lever
Occurrencecongenitaal
SNOMED CT to ICD-10 extended map
TargetE74.0
RuleTRUE
AdviceALWAYS E74.0
CorrelationSNOMED CT source code to target map code correlation not specified