SNOMED Terminos Clinicos

Last uploaded: January 16, 2025

Preferred Name	deficiencia hereditaria de factor V
Synonyms	parahemofilia deficiencia de globulina AC enfermedad de Owren deficiencia hereditaria de factor V (trastorno) hipoproacelerinemia hereditaria
ID	http://purl.bioontology.org/ontology/SCTSPA/88776002
Active	1
altLabel	parahemofilia deficiencia de globulina AC enfermedad de Owren deficiencia hereditaria de factor V (trastorno) hipoproacelerinemia hereditaria
CASE SIGNIFICANCE ID	900000000000020002 900000000000448009 900000000000017005
cui	C0015499
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	88776002
prefLabel	88776002
Subset member	450828004~ACCEPTABILITYID~900000000000549004 450828004~ACCEPTABILITYID~900000000000548007
tui	T047
Type ID	900000000000003001 900000000000013009
subClassOf	http://purl.bioontology.org/ontology/SCTSPA/16922007 http://purl.bioontology.org/ontology/SCTSPA/4320005

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/ICD10CM/D68.2	ICD10CM	CUI
http://purl.bioontology.org/ontology/SNMI/DC-63060	SNMI	CUI
http://purl.bioontology.org/ontology/RCD/D3032	RCD	CUI
http://purl.bioontology.org/ontology/NDFRT/N0000001199	NDFRT	CUI
http://purl.bioontology.org/ontology/MESH/D005166	MESH	CUI
http://purl.bioontology.org/ontology/SNMI/DC-63050	SNMI	CUI
http://purl.bioontology.org/ontology/OMIM/227400	OMIM	CUI
http://purl.bioontology.org/ontology/MSHFRE/D005166	MSHFRE	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/88776002	SNOMEDCT	CUI