Phenotype #0000307096

Individual ID 00415299
Associated disease APBN
Phenotype details Leukodystrophy, spinal cord atrophy, pure motor axonal neuropathy, myopathy
Diagnosis/Initial Adult Polyglucosan Body Disease
Inheritance Familial, autosomal recessive
Diagnosis/Definite Adult Polyglucosan Body Disease
Age/Examination 55y (55 years)
Age/Diagnosis 57y
Age/Onset 54y
Phenotype/Onset 54y
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 09:53:40 +02:00 (CEST)
Date last edited 2022-08-11 13:04:45 +02:00 (CEST)

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