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Results 1 - 10 of 26 for Cataract 6 multiple types
  1. ... 1; FVH1 KERATITIS, HEREDITARY OPTIC NERVE HYPOPLASIA, BILATERAL CATARACT 9, MULTIPLE TYPES; CTRCT9 PAIRED BOX GENE 6; PAX6 NCBI Gene ClinVar Azuma N, Yamaguchi Y, ...
  2. Nystagmus (American Association for Pediatric Ophthalmology and Strabismus)  
    GLOSSARY, TERMS, ACRONYMS, PHRASES, DEFINITIONS, DICTIONARY ... Shows a single glossary entry ... Eye Movement Disorders/Start Here ... Eye Movement Disorders ... American ...
  3. Juvenile Idiopathic Arthritis (JIA) Easy-to-Read From the National Institutes of Health (National Institute of Arthritis and Musculoskeletal and Skin Diseases)  
    Juvenile Arthritis/Start Here ... Juvenile Arthritis ... National Institute of Arthritis and Musculoskeletal and Skin Diseases ... Juvenile arthritis describes arthritis ...
  4. ... aging early in life, such as cloudy lenses (cataracts) in both eyes, skin ... develop multiple, rare cancers during their lifetime. People with Werner ...
  5. ... DJ. Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind ... virus type 1 envelope proteins traffic toward virion assembly sites ...
  6. Diagnosed with NF2-Related Schwannomatosis (Children's Tumor Foundation) - PDF  
    Neurofibromatosis/Specifics ... Neurofibromatosis ... Children's Tumor Foundation ... PDF
  7. ... health, fibromyalgia, IBS, and rare diseases 2024, Issue ... hydration 2024, Issue 3 Download this issue as ...
  8. Usher Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Usher Syndrome/Learn More ... Usher Syndrome ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information ...
  9. Limb Loss/Start Here ... Limb Loss ... Artificial Limbs/Start Here ... Artificial Limbs ... Amputee Coalition ... PDF
  10. ... cell. A mutation that has been found in multiple people with autosomal dominant optic atrophy and cataract results in the production of a protein with ...
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