Skip navigation

Refine by Type

Results 1 - 6 of 6 for Aspartylglycosaminuria
Did you mean aspartylglucosaminuria?
  1. Genetics Home Reference: Aspartylglucosaminuria From the National Institutes of Health (National Library of Medicine)  
    ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Aspartylglucosaminuria On this page: Description Genetic changes Inheritance Diagnosis ...
  2. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... to web site ] [ study information ] [+] Lysosomal Disease Network Aspartylglucosaminuria Batten disease Batten disease: late infantile Bone Disease ...
  3. Developmental Disabilities (National Library of Medicine)  
    Developmental disabilities are severe, long-term problems. They may be physical, such as blindness. They may affect mental ability, such as learning disorders. Or ...
  4. Genetics Home Reference: Seizures From the National Institutes of Health (National Library of Medicine)  
    ... 3 microdeletion Alpers-Huttenlocher syndrome aminoacylase 1 deficiency aspartylglucosaminuria ataxia neuropathy spectrum benign familial neonatal seizures familial ...
  5. 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. ...
  6. Metabolic Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...