SNOMED Terminos Clinicos

Last uploaded: January 16, 2025

Preferred Name	enfermedad de von Willebrand hereditaria tipo 2N
Synonyms	enfermedad de von Willebrand hereditaria tipo 2N (trastorno) enfermedad de von Willebrand tipo 2N
ID	http://purl.bioontology.org/ontology/SCTSPA/359732009
Active	1
altLabel	enfermedad de von Willebrand hereditaria tipo 2N (trastorno) enfermedad de von Willebrand tipo 2N
CASE SIGNIFICANCE ID	900000000000017005
cui	C1282975
DEFINITION STATUS ID	900000000000074008
Effective time	20020131
Focus of	http://purl.bioontology.org/ontology/SCTSPA/408197007
Has interpretation	http://purl.bioontology.org/ontology/SCTSPA/263654008
interprets	http://purl.bioontology.org/ontology/SCTSPA/74848003
Module ID	450829007
notation	359732009
prefLabel	359732009
Subset member	450828004~ACCEPTABILITYID~900000000000549004 450828004~ACCEPTABILITYID~900000000000548007
tui	T047
Type ID	900000000000003001 900000000000013009
subClassOf	http://purl.bioontology.org/ontology/SCTSPA/128107007 http://purl.bioontology.org/ontology/SCTSPA/85995004

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/ICD10CM/D68.023	ICD10CM	CUI
http://purl.bioontology.org/ontology/MESH/D056728	MESH	CUI
http://purl.bioontology.org/ontology/OMIM/613160	OMIM	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/359732009	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/MSHFRE/D056728	MSHFRE	CUI
http://purl.bioontology.org/ontology/OMIM/613554	OMIM	CUI