DEFECTIVE COULOUR VISION

Preferred Label : DEFECTIVE COULOUR VISION;

Origin ID

0237;

UMLS CUI

C0009398;

Currated CISMeF NLP mapping
- Color vision deficiencies [ICD-10 Sub-category]
- Color vision deficiencies [ICD-9 code]
- Color vision deficiency (disorder) [SNOMED CT concept]
- Color-vision disease [ORDO Disease]
- Colour vision deficiencies [ICD-10 Sub-category (who)]
- Defective color vision [MedDRA LLT]
- Defective colour vision [MedDRA LLT]
- Impairment of colour vision [ICD-11 Category]
- color blindness [MedlinePlus Topic]
- color vision defects [MeSH Descriptor]
- color vision defects [MeSH concept]
- color vision defects [Disease (Nov.)]
- color vision deficiency, nos [SNOMED Notion]
Manual NTBT mappings (CISMeF)
- Genetic vitreous-retinal disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Color vision deficiencies [ICD-10 Sub-category]
- Color vision deficiency (disorder) [SNOMED CT concept]
- Color-vision disease [ORDO Disease]
- Colour vision deficiencies [ICD-10 Sub-category (who)]
- Defective color vision [MedDRA LLT]
- Defective colour vision [MedDRA LLT]
- color vision defects [MeSH Descriptor]
- color vision defects [MeSH concept]
- color vision defects [Disease (Nov.)]