Congenital anomaly of large intestine
Congenital hamartoma
Developmental hereditary disorder
Familial multiple polyposis syndrome
Hamartoma of intestine
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Gardner syndrome (disorder)
Gardner syndrome
GS - Gardner's syndrome
Id60876000
StatusPrimitive
Associated morphologyMultiple polyps
Finding siteStructure of large intestine
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyHamartoma
Finding siteStructure of large intestine
OccurrenceCongenital
Global Patient Set
General Practice / Family Practice reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetD12.6
TermBenigne neoplasma van colon, niet gespecificeerd
TargetZ83.7
TermFamilie-anamnese met ziekten van spijsverteringsstelsel
SNOMED CT to ICD-10 extended map
TargetD12.6
RuleTRUE
AdviceALWAYS D12.6 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE
CorrelationSNOMED CT source code to target map code correlation not specified