color blindness

Preferred Label : color blindness;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0004827;

UMLS CUI

C0242225;

Automatic exact mappings (from CISMeF team)
- Blindness colour [MedDRA LLT]
- Color blindness [LOINC component]
- Color blindness NOS [MedDRA LLT]
- Dyschromatopsia [HPO term]
- opsin 1, short wave sensitive [HGNC gene]
Currated CISMeF NLP mapping
- BLINDNESS COLOUR [WHO-ART Preferred Term]
- Blindness color [MedDRA LLT]
- Color Blindness [NCIt concept]
- Color blindness [MedDRA LLT]
- Color blindness (disorder) [SNOMED CT concept]
- Color vision deficiency (disorder) [SNOMED CT concept]
- Colour blindness [MedDRA Preferred Term]
- Colour blindness NOS [MedDRA LLT]
- color blindness [DO Concept]
- color blindness [Disease (Nov.)]
- color blindness [MedlinePlus Topic]
Related record
- color vision defects [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- BLINDNESS COLOUR [WHO-ART Preferred Term]
- Blindness color [MedDRA LLT]
- Blindness colour [MedDRA LLT]
- Color Blindness [NCIt concept]
- Color blindness [MedDRA LLT]
- Color blindness [LOINC component]
- Color blindness (disorder) [SNOMED CT concept]
- Color blindness NOS [MedDRA LLT]
- Color vision deficiencies [ICD-9 code]
- Colour blindness [MedDRA Preferred Term]
- Colour blindness NOS [MedDRA LLT]
- color blindness [MedlinePlus Topic]
- color blindness [DO Concept]
- color vision deficiency, nos [SNOMED Notion]