SNOMED Terminos Clinicos

Last uploaded: January 31, 2024

Preferred Name	deficiencia hereditaria de factor II
Synonyms	deficiencia hereditaria de factor II (trastorno) hipoprotrombinemia hereditaria
ID	http://purl.bioontology.org/ontology/SCTSPA/33297000
Active	1
altLabel	deficiencia hereditaria de factor II (trastorno) hipoprotrombinemia hereditaria
CASE SIGNIFICANCE ID	900000000000448009 900000000000017005
cui	C0272317
DEFINITION STATUS ID	900000000000074008
Effective time	20020131
Has interpretation	http://purl.bioontology.org/ontology/SCTSPA/263654008
interprets	http://purl.bioontology.org/ontology/SCTSPA/74848003
Module ID	450829007
notation	33297000
prefLabel	deficiencia hereditaria de factor II
Subset member	450828004~ACCEPTABILITYID~900000000000549004 450828004~ACCEPTABILITYID~900000000000548007
tui	T047
Type ID	900000000000003001 900000000000013009
subClassOf	http://purl.bioontology.org/ontology/SCTSPA/73975000 http://purl.bioontology.org/ontology/SCTSPA/16922007

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MDRGER/10016076	MDRGER	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/33297000	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/SNMI/DC-63030	SNMI	CUI
http://purl.bioontology.org/ontology/OMIM/613679	OMIM	CUI
http://purl.bioontology.org/ontology/OMIM/176930	OMIM	CUI
http://purl.bioontology.org/ontology/MEDDRA/10016076	MEDDRA	CUI
http://purl.bioontology.org/ontology/MDRFRE/10016076	MDRFRE	CUI
http://purl.bioontology.org/ontology/MESH/C562724	MESH	CUI
http://purl.bioontology.org/ontology/CSP/0438-7564	CRISP	CUI