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Dictionary » Achromatopsia 1
 

Achromatopsia 1

Introduction: Achromatopsia 1

Description of Achromatopsia 1

Achromatopsia 1 (medical condition): A rare form of colorblindness involving complete rod monochromatism which means that that there is no color can be seen and everything appears gray.

See also:

Achromatopsia 1:
  »Introduction: Achromatopsia 1
  »Symptoms of Achromatopsia 1
  »Treatments for Achromatopsia 1

Achromatopsia 1: Related Topics

These medical condition or symptom topics may be relevant to medical information for Achromatopsia 1:

Achromatopsia 1: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Achromatopsia 1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Achromatopsia 1, or a subtype of Achromatopsia 1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Achromatopsia 1 as a Disease

Achromatopsia 1 (medical condition): See Achromatopsia 1 (disease information).
  »Introduction: Achromatopsia 1
  »Symptoms of Achromatopsia 1
  »Treatments for Achromatopsia 1

More information on medical condition: Achromatopsia 1:

Terms associated with Achromatopsia 1:

Terms Similar to Achromatopsia 1:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Chromosome 20, deletion 20p
  • Chromosome 20, duplication 20p
  • Chromosome 20, trisomy
  • Chromosome 20p deletion syndrome
  • Chromosome 20p monosomy
  • Chromosome 20p trisomy
  • Chromosome 20q duplication syndrome
  • Chromosome 21
  • Chromosome 21 monosomy
  • Chromosome 21 monosomy syndrome
  • Chromosome 21 ring
  • Chromosome 21 ring syndrome

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