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Congenital color blindness

disorder
SNOMED 232148006CUI C0339697

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Protan defect(child)
Tritan defect(child)
Achromatopsia(child)
Deutan defect(child)
Blue cone monochromatism(child)
Colour vision deficiency(parent)
No colour perception(parent)
Congenital disease(parent)

Quick Facts

SNOMED CT
232148006
UMLS CUI
C0339697
Fully Specified Name
Congenital color blindness (disorder)
Specialists
0
Diagnostic Biomarkers
0
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.