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familiair syndroom van papillair schildkliercarcinoom met renale papillaire neoplasie (aandoening)
familiair syndroom van papillair schildkliercarcinoom met renale papillaire neoplasie
fPTC/PRN
Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome
An extremely rare inherited tumor syndrome within the familial nonmedullary thyroid cancer group.
Id716657000
StatusDefined
Associated morphologypapillair neoplasma
Finding sitestructuur van nier
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetC73
TermMaligne neoplasma van schildklier
TargetD41.0
TermNeoplasma met onzeker of onbekend gedrag van nier
SNOMED CT to Orphanet simple map97290
SNOMED CT to ICD-10 extended map
TargetC73
RuleTRUE
AdviceALWAYS C73 | MAPPED FOLLOWING WHO GUIDANCE | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE
CorrelationSNOMED CT source code to target map code correlation not specified
TargetD41.0
RuleTRUE
AdviceALWAYS D41.0 | MAPPED FOLLOWING SNOMED GUIDANCE | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE
CorrelationSNOMED CT source code to target map code correlation not specified