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Results 1 - 10 of 17 for Angiokeratoma corporis diffusum
  1. ... disease. Alpha-galactosidase A deficiency Anderson-Fabry disease Angiokeratoma corporis diffusum Angiokeratoma diffuse Ceramide trihexosidase deficiency Fabry's disease ...
  2. ... type Alpha-N-acetylgalactosaminidase deficiency Alpha-NAGA deficiency Angiokeratoma corporis diffusum-glycopeptiduria GALB deficiency Kanzaki disease Lysosomal glycoaminoacid storage ...
  3. Fabry Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Lipid Metabolism Disorders/Specifics ... Lipid Metabolism Disorders ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... National Institute of Neurological ...
  4. ... A, Ne'eman Z, Zeigler M, Zlotogorski A. Angiokeratoma corporis diffusum in human beta-mannosidosis: Report of a new ...
  5. ... A, Ne'eman Z, Zeigler M, Zlotogorski A. Angiokeratoma corporis diffusum in human beta-mannosidosis: Report of a new ...
  6. ... GLA gene have been identified in people with Fabry disease. Most of these genetic changes are unique to ... leading to the varied signs and symptoms of Fabry disease.Mutations that eliminate the activity of the alpha- ...
  7. Pegunigalsidase alfa-iwxj injection is used to treat Fabry disease (an inherited condition in which a type of ...
  8. Agalsidase beta injection is used to treat Fabry disease (an inherited condition in which a type of fatty substance builds up in the body, resulting in nerve and organ damage) in adults ...
  9. Lipid Storage Diseases From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Gaucher Disease/Learn More ... Gaucher Disease ... Lipid Metabolism Disorders/Start Here ... Lipid Metabolism Disorders ... Tay-Sachs Disease/Related Issues ... Tay-Sachs Disease
  10. 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. ...
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