SNOMED Clinical Terms - Accessory spleen - Terms

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Preferred Name	Accessory spleen
Synonyms	Polysplenia Splenunculi Supernumerary spleen Accessory spleen (disorder)
ID	10362008
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/10362008
CONCEPTSTATUS	0
CTV3ID	PK02.
has_associated_morphology	Supernumerary structure
has_clinical_course	Courses
has_finding_site	Splenic structure
has_severity	Severities
isa	Congenital malformation Congenital anomaly of spleen
ISPRIMITIVE	0
occurs_in	Congenital
Semantic_Type	Congenital Abnormality
SNOMEDID	D4-C1002
SYNONYM FN	Accessory spleen (disorder)
SYNONYM SY	Polysplenia Splenunculi Supernumerary spleen
TUI	T019
UMLS_CUI	C0266631

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.obolibrary.org/obo/HP_0001747	Human Phenotype Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU014796	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0266631	skos:closeMatch	loom	05/21/13	View Notes
http://bioontology.org/projects/ontologies/radlex/radlexOwlDlComponent#RID33457	RadLex	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.obolibrary.org/obo/HP_0001748	Human Phenotype Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:1157	Fanconi Anemia (FA) Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.org/obo/owl/HP#HP_0001747	Bone Dysplasia Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU006865	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU006865	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0266631	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/PK02.	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0266631	skos:closeMatch	loom	05/21/13	View Notes
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:1160	Fanconi Anemia (FA) Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU009634	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0266631	skos:closeMatch	loom	05/21/13	View Notes
http://www.co-ode.org/ontologies/galen#AccessorySpleen	Galen	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU016582	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/PK02.	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://uwhealth.org/himc/icd/icd09/#759.0	ICD09	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU016582	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0266631	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MDR/10068059	MedDRA	NLM UMLS (CUI)	CUI: C0266631	skos:closeMatch	loom	05/21/13	View Notes
http://purl.org/obo/owl/MP#MP_0003342	Suggested Ontology for Pharmacogenomics	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.org/obo/owl/HP#HP_0001748	Bone Dysplasia Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU009634	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.obolibrary.org/obo/MP_0003342	Mammalian phenotype	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.org/obo/owlapi/fma#FMA_16028	BioModels Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MDR/10068059	MedDRA	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes

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