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ACHM1

Introduction: ACHM1

Description of ACHM1

ACHM1 (medical condition): A rare form of colorblindness involving complete rod monochromatism which means...more »

See also:

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

ACHM1: Rare Disease

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

ACHM1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that ACHM1, or a subtype of ACHM1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

ACHM1 as a Disease

ACHM1: Another name for Achromatopsia 1 (or close medical condition association).
  »Introduction: Achromatopsia 1
  »Symptoms of Achromatopsia 1
  »Treatments for Achromatopsia 1

ACHM1: Related Diseases

ACHM1: ACHM1 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of ACHM1 (Achromatopsia 1)

Some of the symptoms of ACHM1 incude:

  • Head posture against strong light
  • Absence of photopic flicker
  • Very few cones
  • No cones
  • Depigmented cones

Treatments for ACHM1 (Achromatopsia 1)

Treatments for ACHM1 (Achromatopsia 1) include:

  • There is no specific treatment for the condition other than using proper eye-glasses to assist with any vision defects. Tinted glasses may help with light sensitivity

Treatment of ACHM1: For more treatment information about ACHM1, see treatment of Achromatopsia 1 (ACHM1)

Terms associated with ACHM1:

Terms Similar to ACHM1:

Source - NIH

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