Phenotype #0000000929

Individual ID 00001775
Associated disease EDS
Inheritance Unknown
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Onset 35y
Phenotype/Onset -
Phenotype details ascertainment ; clinical presentation; optic atrophy, ataxia, spasticity
Hearing/Loss -
Protein -
CK-level -
EMG -
Muscle/Biopsy -
Age/Diagnosis -
Owner name Division of Human Genetics, Innsbruck
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Division of Human Genetics, Innsbruck
Date created 2011-06-07 16:51:06 +02:00 (CEST)
Date last edited 2013-04-07 17:59:38 +02:00 (CEST)

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