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Hereditary hemoglobinopathy due to globin chain mutation (disorder)
Hereditary hemoglobinopathy due to globin chain mutation
Structural hemoglobinopathy
hereditaire hemoglobinopathie door mutatie in globineketen
erfelijke hemoglobinopathie door mutatie in globineketen
structurele hemoglobinopathie
Id127038008
StatusPrimitive
Finding siteErythrocyte
OccurrenceCongenital
ICD-10 complex map reference set
TargetD58.2
RuleTRUE
AdviceALWAYS D58.2
CorrelationSNOMED CT source code to target map code correlation not specified
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