Global Variome shared LOVD

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Phenotype #0000050865 Individual ID 00064665 Associated disease SPG Phenotype details see paper; .., lower-extremity spasticity, lower-extremity weakness, lower-extremity hyperreflexia, extensor plantar response, abnormal bladder function, foot deformity, dysarthria, upper extremity hyperreflexia Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 31y (31 years) Age/Diagnosis - Age/Onset 20y Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2016-05-07 21:23:24 +02:00 (CEST) Date last edited 2016-05-07 21:30:49 +02:00 (CEST)

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