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Results 1 - 7 of 7 for Myopia "23," autosomal recessive
  1. Nearsightedness 
    ... X-LINKED; MYP1 MYOPIA 13, X-LINKED; MYP13 MYOPIA 18, AUTOSOMAL RECESSIVE; MYP18 MYOPIA 3, AUTOSOMAL DOMINANT; MYP3 MYOPIA 6; MYP6 MYOPIA 17, AUTOSOMAL ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  2. Autosomal recessive congenital stationary night blindness 
    ... blindness can interfere with other visual systems, causing myopia, reduced visual acuity, and other impairments.Some people with autosomal recessive congenital stationary night blindness have no identified mutation ...
    https://medlineplus.gov/...ive-congenital-stationary-night-blindness - Genetics
  3. Sick sinus syndrome 
    ... The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show ... ClinicalTrials.gov ...
    https://medlineplus.gov/genetics/condition/sick-sinus-syndrome - Genetics
  4. Usher Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Usher Syndrome/Learn More ... Usher Syndrome ... Find symptoms and other information about Usher syndrome. ... Genetic and Rare Diseases Information Center ... From the National ...
    https://rarediseases.info.nih.gov/diseases/7843/usher-syndrome - External Health Links
  5. Sjögren-Larsson syndrome 
    ... fats. ALDH3A2 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/genetics/condition/sjogren-larsson-syndrome - Genetics
  6. Knobloch syndrome 
    ... symptoms. COL18A1 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/genetics/condition/knobloch-syndrome - Genetics
  7. Cohen syndrome 
    ... syndrome. VPS13B This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/genetics/condition/cohen-syndrome - Genetics