Phenotype #0000138579

Individual ID 00170838
Associated disease spastic ataxia
Diagnosis/Initial Spastic Ataxia
Diagnosis/Definite -
Phenotype details Gait and speech difficulties, Saccadic pursuit, UL & LL ataxia, LL spasticity, wheelchair, Normal cognitive state
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Onset 20y
Phenotype/Onset -
Protein -
Owner name Inge Meijer
Database submission license No license selected
Created by Inge Meijer
Date created 2018-07-27 21:07:54 +02:00 (CEST)
Date last edited N/A

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