SNOMED Terminos Clinicos

Last uploaded: January 31, 2024

Preferred Name	coproporfiria hereditaria
Synonyms	sÃndrome de Berger - Goldberg deficiencia de CPO deficiencia de CPRO coproporfiria hereditaria (trastorno) porfiria hepÃ¡tica II
ID	http://purl.bioontology.org/ontology/SCTSPA/7425008
Active	1
altLabel	sÃndrome de Berger - Goldberg deficiencia de CPO deficiencia de CPRO coproporfiria hereditaria (trastorno) porfiria hepÃ¡tica II
CASE SIGNIFICANCE ID	900000000000020002 900000000000448009 900000000000017005
cui	C0162531
DEFINITION STATUS ID	900000000000073002
Effective time	20200731
Has finding site	http://purl.bioontology.org/ontology/SCTSPA/10200004
Module ID	450829007
notation	7425008
prefLabel	coproporfiria hereditaria
Subset member	450828004~ACCEPTABILITYID~900000000000549004 450828004~ACCEPTABILITYID~900000000000548007
tui	T047
Type ID	900000000000003001 900000000000013009
subClassOf	http://purl.bioontology.org/ontology/SCTSPA/190915002 http://purl.bioontology.org/ontology/SCTSPA/55056006 http://purl.bioontology.org/ontology/SCTSPA/363080007

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/NDFRT/N0000011116	NDFRT	CUI
http://purl.bioontology.org/ontology/MEDDRA/10019866	MEDDRA	CUI
http://purl.bioontology.org/ontology/OMIM/121300	OMIM	CUI
http://purl.bioontology.org/ontology/MSHFRE/D046349	MSHFRE	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/7425008	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/CSP/1849-7674	CRISP	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU071250	OMIM	CUI
http://purl.bioontology.org/ontology/RCD/Xa01L	RCD	CUI
http://purl.bioontology.org/ontology/RCD/X40WU	RCD	CUI
http://purl.bioontology.org/ontology/MDRFRE/10019866	MDRFRE	CUI
http://purl.bioontology.org/ontology/MESH/D046349	MESH	CUI
http://purl.bioontology.org/ontology/SNMI/D6-88320	SNMI	CUI
http://purl.bioontology.org/ontology/MDRGER/10019866	MDRGER	CUI
http://purl.bioontology.org/ontology/ICD10CM/E80.29	ICD10CM	CUI