Phenotype #0000157554

Individual ID 00208947
Associated disease EAOH
Phenotype details cerebellar ataxia, ocular apraxia, ...(not complete clinical information).
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 Sergio Piñeiro
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Rick van Minkelen
Date created 2013-06-07 11:18:43 +02:00 (CEST)
Date last edited 2015-07-29 15:45:36 +02:00 (CEST)

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