Phenotype #0000307090

Individual ID 00415292
Associated disease APBN
Phenotype details Leukodystrophy, spinal cord atrophy, peripheral neuropathy, myopathy
Diagnosis/Initial Adult Polyglucosan Body Disease
Inheritance Familial, autosomal recessive
Diagnosis/Definite Adult Polyglucosan Body Disease
Age/Examination 49y (49 years)
Age/Diagnosis 53y
Age/Onset 47y
Phenotype/Onset -
Protein -
Owner name Jonathan De Winter
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Jonathan De Winter
Date created 2022-08-11 09:30:19 +02:00 (CEST)
Date last edited 2022-08-11 13:03:50 +02:00 (CEST)

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