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Diseases » Achromatopsia 3 » Summary
 

What is Achromatopsia 3?

What is Achromatopsia 3?

  • Achromatopsia 3: A rare form of colorblindness which also involves myopia.

Achromatopsia 3 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Achromatopsia 3, or a subtype of Achromatopsia 3, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Achromatopsia 3: Introduction

Types of Achromatopsia 3:

Broader types of Achromatopsia 3:

What causes Achromatopsia 3?

Causes of Achromatopsia 3: see causes of Achromatopsia 3

What are the symptoms of Achromatopsia 3?

Symptoms of Achromatopsia 3: see symptoms of Achromatopsia 3

Achromatopsia 3: Testing

Diagnostic testing: see tests for Achromatopsia 3.

Misdiagnosis: see misdiagnosis and Achromatopsia 3.

How is it treated?

Doctors and Medical Specialists for Achromatopsia 3: Medical Geneticist, Ophthalmologist ; see also doctors and medical specialists for Achromatopsia 3.
Treatments for Achromatopsia 3: see treatments for Achromatopsia 3

Name and Aliases of Achromatopsia 3

Main name of condition: Achromatopsia 3

Other names or spellings for Achromatopsia 3:

Pingelapese, ACHM 3, Achromatopsia with myopia, Total colorblindness with myopia, Formerly Rod Monochromatism 1

ACHM 3, Achromatopsia with myopia, Pingelapese, Total colorblindness with myopia
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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