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)