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Potassium inwardly rectifying channel subfamily J member 11 gene related ATP-sensitive potassium channel pore-forming subunit deficiency (disorder)
KCNJ11 gene related ATP-sensitive potassium channel pore-forming subunit deficiency
Potassium inwardly rectifying channel subfamily J member 11 gene related ATP-sensitive potassium channel pore-forming subunit deficiency
Kir6.2 deficiency
Id1407029008
StatusPrimitive
SNOMED CT to ICD-10 extended map
Target
RuleTRUE
AdviceMAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
CorrelationSNOMED CT source code to target map code correlation not specified