Phenotype #0000332776

Individual ID 00443435
Associated disease ?
Diagnosis/Initial ataxia with oculomotor apraxia
Diagnosis/Definite EAOH
Phenotype details progressive loss of ambulation, intellectual disability
Inheritance Familial, autosomal recessive
Age/Examination 40y (40 years)
Age/Diagnosis -
Age/Onset 16y
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-11-26 13:31:49 +01:00 (CET)
Date last edited N/A

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