Hereditary thrombophilia
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Prothrombin G20210A mutation (disorder)
Prothrombin G20210A mutation
protrombine-G20210A-mutatie
G20210A-mutatie van bloedstollingsfactor II
protrombinemutatie G20210A
G20210A-mutatie van protrombine
G20210A-mutatie van factor II
mutatie van protrombine G20210A
G20210A-mutatie van stollingsfactor II
Id440989002
StatusPrimitive
Has interpretationAbnormal
InterpretsHemostatic function
ICD-10 complex map reference set
TargetD68.5
RuleTRUE
AdviceALWAYS D68.5
CorrelationSNOMED CT source code to target map code correlation not specified
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Heterozygous prothrombin G20210A mutation
Homozygous prothrombin G20210A mutation