Phenotype #0000157571

Individual ID 00208964
Associated disease EAOH
Phenotype details psychomotor retardation, epilepsy, clinically AOA1 (no details provided by requesting physician).
Diagnosis/Initial Ataxia-ocular apraxia type 1
Inheritance Unknown
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 2013-11-07 14:18:41 +01:00 (CET)
Date last edited 2015-07-30 10:01:42 +02:00 (CEST)

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