SNOMED Clinical Terms - Central scotoma - Terms

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Preferred Name	Central scotoma
Synonyms	Scotoma of central area Central loss of vision Central scotoma (finding)
ID	38950008
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/38950008
CONCEPTSTATUS	0
CTV3ID	F4841
has_clinical_course	Courses
has_episodicity	Episodicities
has_finding_site	Eye region structure
has_severity	Severities
inverse_was_a	Central area scotoma NOS
isa	Visual field scotoma Head finding
ISPRIMITIVE	1
Semantic_Type	Finding
SNOMEDID	DA-74610
SYNONYM FN	Central scotoma (finding)
SYNONYM IS	Scotoma of central area
SYNONYM SY	Central loss of vision
TUI	T033
UMLS_CUI	C0152191

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.org/obo/owl/HP#HP_0000603	Bone Dysplasia Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/H53.41	International Classification of Diseases, Version 10 - Clinical Modfication	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/F4841	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/CST/VISUAL%20FIELD%20DEFECT	Coding Symbols for a Thesaurus of Adverse Reaction Terms	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MDR/10007973	Medical Dictionary for Regulatory Activities	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:0249	Fanconi Anemia Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/H53.41	International Classification of Diseases, Version 10 - Clinical Modfication	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU009884	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU000024	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/WHO/0147	WHO Adverse Reaction Terminology	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/F4844	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/F4841	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MDR/10007973	Medical Dictionary for Regulatory Activities	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MSH/D012607	Medical Subject Headings	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU000024	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://uwhealth.org/himc/icd/icd09/#368.41	International Classification of Diseases, Version 9	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/ICD9CM/368.41	International Classification of Diseases, Version 9 - Clinical Modification	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MSH/D012607	Medical Subject Headings	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MDR/10039732	Medical Dictionary for Regulatory Activities	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MDR/10039731	Medical Dictionary for Regulatory Activities	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU002535	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU030348	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes
http://purl.obolibrary.org/obo/HP_0000603	Human Phenotype Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/ICD9CM/368.41	International Classification of Diseases, Version 9 - Clinical Modification	NLM UMLS (CUI)	CUI: C0152191	skos:closeMatch	loom	05/21/13	View Notes

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