familiaire aandoening
stollingsstoornis
||
familiaire afwijking van trombomoduline (aandoening)
familiaire afwijking van trombomoduline
Familial thrombomodulin anomalies
A rare, life-threatening, genetic coagulation disorder characterized by an increased risk of blood clot formation in several members of a family due to a thrombomodulin gene mutation. Patients may manifest with venous thromboembolic disease, premature myocardial infarction and/or arterial thrombosis.
Id783256001
StatusPrimitive
Has interpretationafwijkend
Interpretshemostase
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetD68.8
TermOverige gespecificeerde stollingsstoornissen
SNOMED CT to Orphanet simple map3324
SNOMED CT to ICD-10 extended map
TargetD68.8
RuleTRUE
AdviceALWAYS D68.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified