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Results 1 - 10 of 45 for "Cataracts," Autosomal Dominant
  1. Autosomal dominant optic atrophy and cataract 
    ... 3 OPA3 OPA3, autosomal dominant Optic atrophy and cataract, autosomal dominant Optic atrophy type 3 Optic atrophy, cataract, and ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics
  2. Autosomal dominant vitreoretinochoroidopathy 
    ... ADVIRC Vitreoretinochoroidopathy dominant Vitreoretinochoroidopathy with microcornea, glaucoma, and cataract Vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos Genetic Testing Registry: Autosomal dominant vitreoretinochoroidopathy ...
    https://medlineplus.gov/...osomal-dominant-vitreoretinochoroidopathy - Genetics
  3. OPA3 gene 
    ... the OPA3 gene have been found to cause autosomal dominant optic atrophy and cataract. This condition causes slowly worsening vision in both ... problems.Mutations in the OPA3 gene that cause autosomal dominant optic atrophy and cataract occur in one copy of the gene in ...
    https://medlineplus.gov/genetics/gene/opa3 - Genetics
  4. Cataract (National Library of Medicine)  
    A cataract is a clouding of the lens in your eye. It affects your vision. Cataracts are very common in older people. By age 80, more than half of all Americans ...
    https://medlineplus.gov/cataract.html - Health Topics
  5. Optic Nerve Disorders (National Library of Medicine)  
    The optic nerve is a bundle of more than 1 million nerve fibers that carry visual messages. You have one connecting the back of each eye (your retina) to ...
    https://medlineplus.gov/opticnervedisorders.html - Health Topics
  6. Fibrochondrogenesis 
    ... 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
  7. ALDH18A1 gene 
    ... joints; clouding of the lenses of the eyes (cataracts) or other eye abnormalities; intellectual disability; and movement problems that can worsen over time. Autosomal recessive cutis laxa tends to be more severe than autosomal dominant.Most ALDH18A1 gene variants involved in cutis laxa ...
    https://medlineplus.gov/genetics/gene/aldh18a1 - Genetics
  8. About Myotonic Dystrophy From the National Institutes of Health (National Human Genome Research Institute)  
    Myotonic dystrophy is an inherited type of muscular dystrophy that affects the muscles and other body systems. ... Muscular Dystrophy/Genetics ... Muscular Dystrophy
    https://www.genome.gov/Genetic-Disorders/Myotonic-Dystrophy - External Health Links
  9. Hyperferritinemia-cataract syndrome 
    ... formed. FTL ... syndrome HHCS Genetic Testing Registry: ...
    https://medlineplus.gov/.../hyperferritinemia-cataract-syndrome - Genetics
  10. Muscular Dystrophy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Muscular Dystrophy/Start Here ... Muscular Dystrophy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Muscular dystrophy ( ...
    https://www.ninds.nih.gov/.../disorders/muscular-dystrophy - External Health Links
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