familiaire aandoening
stollingsstoornis
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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
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