Impairment of colour vision

ICD-11 code : 9D44;

Preferred Label : Impairment of colour vision;

ICD-11 definition : Colour vision refers to the ability to distinguish colour differences. True colour blindness is extremely rare. Most colour vision deficiencies are minor, and congenital, with X-linked recessive inheritance (more prevalent among men). Some drugs and optic neuritis may also cause colour vision deficiencies.;

ICD-11 synonym : monochromatism; colour vision deficiency; protan defect; achromatism; colour blindness; total colour blindness; congenital colour blindness; complete colour blindness; achromatopsia; acquired colour vision deficiency; acquired colour blindness;

ICD-11 inclusion : achromatopsia; colour blindness; acquired colour vision deficiency;

Details

Origin ID

2028524981;

Automatic exact mappings (from CISMeF team)
- Achromatopsia [ICD-9 code]
- Acquired color vision deficiency (disorder) [SNOMED CT concept]
- Blindness colour [MedDRA LLT]
- Colour blindness acquired [MedDRA Preferred Term]
- Daltonism [MedDRA LLT]
- Daltonism (disorder) [SNOMED CT concept]
- Deutan defect (disorder) [SNOMED CT concept]
- Monochromatic (qualifier value) [SNOMED CT concept]
- Monochromatism [PASCAL descriptor]
- Other specified or unknown diagnosis or diseases of eye and adnexa [ICPC-3 diagnosis]
- Partial color blindness, protan type [ORDO Disease]
- Protan defect [MedDRA LLT]
- Protan defect [ICD-9 code]
- Protan defect (disorder) [SNOMED CT concept]
- Protanopia [PASCAL descriptor]
- Protanopia [HPO term]
- acquired color blindness [DO Concept]
- deutan defect [SNOMED Notion]
- eye/adnexa disease other [ICPC-2 Rubric]
- monochromatic [SNOMED Notion]
- protan defect [SNOMED Notion]
- red color blindness [DO Concept]
Currated CISMeF NLP mapping
- Achromatopsia [PASCAL descriptor]
- Achromatopsia [HPO term]
- Achromatopsia [MedDRA LLT]
- Achromatopsia [NCIt concept]
- Achromatopsia (disorder) [SNOMED CT concept]
- BLINDNESS COLOUR [WHO-ART Preferred Term]
- Blindness color [MedDRA LLT]
- Blindness colour total [MedDRA LLT]
- Color blindness (disorder) [SNOMED CT concept]
- Color vision deficiencies [ICD-9 code]
- Color vision deficiencies [ICD-10 Sub-category]
- Color vision deficiency (disorder) [SNOMED CT concept]
- Color-vision disease [ORDO Disease]
- Colour blindness [MedDRA Preferred Term]
- Colour vision deficiencies [ICD-10 Sub-category (who)]
- DEFECTIVE COULOUR VISION [WHO-ART Included Term]
- Defective color vision [MedDRA LLT]
- Defective colour vision [MedDRA LLT]
- achromatopsia [SNOMED Notion]
- achromatopsia [MeSH concept]
- achromatopsia [DO Concept]
- color blindness [MedlinePlus Topic]
- color blindness [DO Concept]
- color vision defects [MeSH concept]
- color vision defects [MeSH Descriptor]
- color vision defects [Disease (Nov.)]
- color vision deficiency, nos [SNOMED Notion]
ICD-10 Mapping
- Color vision deficiencies [ICD-10 Sub-category]
Validated automatic mappings to BTNT
- Achromatopsia [ORDO Disease]
- Complete achromatopsia (disorder) [SNOMED CT concept]
- Congenital color blindness (disorder) [SNOMED CT concept]

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