C2931365_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	A rare life-threatening genetic coagulation disorder with characteristics of 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.
?:hasCUIAnnotation	<https://research.tib.eu/covid-19/entity/C2931365>
?:hasGeneratedBy	<https://research.tib.eu/covid-19/SourceName/SNOMEDCT_US>
?:type	<https://research.tib.eu/covid-19/vocab/AnnotationDefinition>

Metadata

Anon_0

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Anon_0

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Anon_1 (more)

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