abnormal vision

Preferred Label : abnormal vision;

Origin ID

F-F0002;

UMLS CUI

C0042790;

Automatic exact mappings (from CISMeF team)
- Abnormal Vision [NCIt concept]
- Abnormal vision [ICD-11 More detail]
- Abnormality of vision [HPO term]
- ELAV like RNA binding protein 1 [HGNC gene]
CISMeF manual mappings
- Dim vision (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Abnormal vision [MedDRA LLT]
- Abnormal vision (finding) [SNOMED CT concept]
- Abnormal vision NOS [MedDRA LLT]
- Vision abnormal [MedDRA LLT]
- Vision abnormal NOS [MedDRA LLT]
- Visual alteration [LOINC component]
- Visual impairment [MedDRA Preferred Term]
- Visual impairment (disorder) [SNOMED CT concept]
SNOMED CT concept
- Abnormal vision (finding) [SNOMED CT concept]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Disorder of vision (disorder) [SNOMED CT concept]
- VISION DISORDERS [WHO-ART Class]
- Vision Disorder [NCIt concept]
- Vision disorder [PASCAL descriptor]
- Vision disorders [MedDRA High Level Group Term]
- Visual system disorder (disorder) [SNOMED CT concept]
- vision disorders [MeSH Descriptor]
- vision disorders [MeSH concept]
- visual disorder [Disease (Nov.)]