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Results 1 - 10 of 19 for Myopia "5," autosomal dominant
  1. Nearsightedness 
    ... MYOPIA 6; MYP6 MYOPIA 17, AUTOSOMAL DOMINANT; MYP17 MYOPIA 5, AUTOSOMAL DOMINANT; MYP5 MYOPIA 7; MYP7 MYOPIA 8; MYP8 MYOPIA 9; MYP9 ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  2. Learning about Marfan Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Marfan Syndrome/Start Here ... Marfan Syndrome ... Marfan syndrome an inherited disorder of connective tissue occurring once in every 10,000 to 20,000 individuals.
    https://www.genome.gov/Genetic-Disorders/Marfan-Syndrome - External Health Links
  3. Sick sinus syndrome 
    ... 1 Genetic Testing Registry: Sick sinus syndrome 2, autosomal dominant Genetic Testing Registry: Sick sinus syndrome 3, susceptibility to Sinus node disease and myopia National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/genetics/condition/sick-sinus-syndrome - Genetics
  4. Stickler syndrome 
    ... type 4 Genetic Testing Registry: Stickler syndrome, type 5 Marshall ... OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; OSMEDA STICKLER SYNDROME, TYPE II; STL2 STICKLER SYNDROME, ...
    https://medlineplus.gov/genetics/condition/stickler-syndrome - Genetics
  5. Fibrochondrogenesis 
    ... related to the condition, including slightly short stature, myopia, cataracts, joint pain, and hearing loss.In at least one case of fibrochondrogenesis caused by a COL11A2 gene mutation, the condition was inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/fibrochondrogenesis - Genetics
  6. Eye Diseases (National Library of Medicine)  
    Some eye problems are minor and don't last long. But some can lead to a permanent loss of vision. Common eye problems include: Refractive errors Cataracts - ...
    https://medlineplus.gov/eyediseases.html - Health Topics
  7. Weill-Marchesani syndrome 
    ... V. In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome. J Med Genet. 2003 Jan; ...
    https://medlineplus.gov/genetics/condition/weill-marchesani-syndrome - Genetics
  8. Isolated ectopia lentis 
    ... the FBN1 gene, it is inherited in an autosomal dominant pattern, which means one copy of the altered ... recessive Genetic Testing Registry: Ectopia lentis 1, isolated, autosomal dominant Isolated ectopia lentis National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/isolated-ectopia-lentis - Genetics
  9. Coloboma 
    ... patterns. Isolated coloboma is sometimes inherited in an autosomal dominant pattern, which means one copy of an altered ... inheritance pattern for that condition, which may be autosomal dominant, autosomal recessive, or X-linked. Congenital ocular coloboma ...
    https://medlineplus.gov/genetics/condition/coloboma - Genetics
  10. Myhre syndrome 
    ... syndrome. SMAD4 Myhre syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/myhre-syndrome - Genetics
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