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Results 1 - 10 of 65 for Genetic prion diseases
  1. Genetics Home Reference: Prion disease From the National Institutes of Health (National Library of Medicine)  
    ... Disease Foundation: Suggestions for Patient Care Gene Review: Genetic Prion Diseases Genetic Testing Registry: Genetic prion diseases MedlinePlus Encyclopedia: ...
  2. Creutzfeldt-Jakob Disease (National Library of Medicine)  
    Creutzfeldt-Jakob disease (CJD) is a rare, degenerative brain disorder. Symptoms usually start around age 60. Memory problems, behavior changes, vision problems, ...
  3. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
  4. Genetics Home Reference: Neuromyelitis optica From the National Institutes of Health (National Library of Medicine)  
    Neuromyelitis optica References Quick links to this topic MedlinePlus Health information Genetic and Rare Diseases Information Center Information about genetic conditions ...
  5. Genetics Home Reference: Sandhoff disease From the National Institutes of Health (National Library of Medicine)  
    Sandhoff disease Related Gene(s) References Quick links to this topic MedlinePlus Health information Genetic and Rare Diseases Information Center Information ...
  6. Alpers-Huttenlocher syndrome Related Gene(s) References Quick links to this topic MedlinePlus Health information Genetic and Rare Diseases Information Center ...
  7. GM2-gangliosidosis, AB variant Related Gene(s) References Quick links to this topic MedlinePlus Health information Additional NIH Resources National Institutes ...
  8. AMACR deficiency Related Gene(s) References Quick links to this topic MedlinePlus Health information Educational resources Information pages Patient support ...
  9. Infantile-onset ascending hereditary spastic paralysis Related Gene(s) References Quick links to this topic MedlinePlus Health information Additional NIH Resources ...
  10. Infantile neuroaxonal dystrophy Related Gene(s) Related Condition(s) References Quick links to this topic MedlinePlus Health information Genetic and Rare Diseases ...
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