Phenotype #0000306800

Individual ID 00414999
Associated disease OPA
Phenotype details see paper; ..., bilateral slowly progressive vision loss
Diagnosis/Initial optic atrophy
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Birth_Details -
MotorSkills -
Vision/Abnormality -
Hearing/Loss -
Eye/Optic_Disc -
Protein -
Brain/Imaging -
Eye/OCT -
Vision/Field -
Vision/Acuity -
Vision/Colour -
Habits -
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 2022-08-05 17:24:11 +02:00 (CEST)
Date last edited 2022-08-05 17:27:45 +02:00 (CEST)

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