Phenotype #0000157583

Individual ID 00208976
Associated disease EAOH
Phenotype details mild scoliosis, nystagmus, mild tremor, gait ataxia, areflexia
Diagnosis/Initial Ataxia-ocular apraxia type 1
Inheritance Familial, autosomal recessive
Diagnosis/Definite EAOH
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Rick van Minkelen
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Rick van Minkelen
Date created 2014-12-11 14:56:48 +01:00 (CET)
Date last edited 2015-07-30 10:41:45 +02:00 (CEST)

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