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
Create New Mapping

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 MedDRA 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 MedDRA NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/MSH/D012607 Medical Subject Headings (MeSH) 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 (MeSH) NLM UMLS (CUI) CUI: C0152191 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/MDR/10039732 MedDRA NLM UMLS (CUI) CUI: C0152191 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/MDR/10039731 MedDRA 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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