Hereditary factor XI deficiency disease
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Factor XI deficiency, type II (disorder)
Factor XI deficiency, type II
Id33169001
StatusPrimitive
OccurrenceCongenital
Has interpretationAbnormal
InterpretsHemostatic function
SNOMED CT to ICD-10 extended map
TargetD68.1
RuleTRUE
AdviceALWAYS D68.1
CorrelationSNOMED CT source code to target map code correlation not specified