Skip navigation

Refine by Type

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. ... the general public. MedlinePlus - Health information Health Topic: Degenerative Nerve Diseases Genetic and Rare Diseases Information Center - Information about genetic ...
  5. ... healthcare provider, see How can I find a genetics professional in my area? in the ... NIH Resources - National Institutes of Health National ...
  6. 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 ...
  7. Genetics Home Reference: Multiple system atrophy From the National Institutes of Health (National Library of Medicine)  
    Multiple system atrophy Related Gene(s) Related Condition(s) References Quick links to this topic MedlinePlus Health information Genetic and Rare Diseases Information ...
  8. Genetics Home Reference: Juvenile Batten disease From the National Institutes of Health (National Library of Medicine)  
    Juvenile Batten disease Related Gene(s) Related Condition(s) References Quick links to this topic MedlinePlus Health information Genetic and Rare Diseases Information ...
  9. Infantile neuronal ceroid lipofuscinosis Related Gene(s) Related Condition(s) References Quick links to this topic MedlinePlus Health information Additional NIH ...
  10. GM2-gangliosidosis, AB variant Related Gene(s) References Quick links to this topic MedlinePlus Health information Additional NIH Resources National Institutes ...
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · next