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Acquired color blindness

MedGen UID:
57828
•Concept ID:
C0155018
•
Disease or Syndrome
Synonyms: Acquired Color Blindness; Color Blindness, Acquired
SNOMED CT: Acquired color vision deficiency (71676008); Acquired color blindness (71676008)
 
Monarch Initiative: MONDO:0001828

Definition

Non-heritable difficulty in distinguishing colors. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVAcquired color blindness

Professional guidelines

PubMed

Dysthyroid optic neuropathy: Demographics, risk factors, investigations, and management outcomes.
Poonam NS, Alam MS, Oberoi P, Mukherjee B
Indian J Ophthalmol 2022 Dec;70(12):4419-4426. doi: 10.4103/ijo.IJO_719_22. PMID: 36453357Free PMC Article
Revealing How Color Vision Phenotype and Genotype Manifest in Individual Cone Cells.
Zhang F, Kurokawa K, Bernucci MT, Jung HW, Lassoued A, Crowell JA, Neitz J, Neitz M, Miller DT
Invest Ophthalmol Vis Sci 2021 Feb 1;62(2):8. doi: 10.1167/iovs.62.2.8. PMID: 33544131Free PMC Article
Diagnosis and Treatment Options for Achromatopsia: A Review of the Literature.
Pascual-Camps I, Barranco-Gonzalez H, Aviñó-Martínez J, Silva E, Harto-Castaño M
J Pediatr Ophthalmol Strabismus 2018 Mar 1;55(2):85-92. Epub 2017 Dec 19 doi: 10.3928/01913913-20171117-01. PMID: 29257187

Supplemental Content

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