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Myopia "28," autosomal recessive
- ... X-LINKED; MYP1 MYOPIA 13, X-LINKED; MYP13 MYOPIA 18, AUTOSOMAL RECESSIVE; MYP18 MYOPIA 3, AUTOSOMAL DOMINANT; MYP3 MYOPIA 6; MYP6 MYOPIA 17, AUTOSOMAL ...
- ... the GRM6 gene have been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see in low light and other vision problems such as nearsightedness (myopia). Most GRM6 gene mutations impair the function of ...
- ... mutations. The parents of an individual with an autosomal recessive condition ... short stature, myopia, cataracts, joint pain, and hearing loss.In at ...
- ... 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 ...
- ... functioning. OAT 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 ...
- ... 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 ...
- ... penetrance.Keratoconus can also be inherited in an autosomal recessive pattern, which means variants occur in both copies ... cell. The parents of an individual with an autosomal recessive condition each carry one copy of the altered ...
- ... syndrome. LRP2 This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ... cases, the parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...