Phenotype #0000278152

Individual ID 00384367
Associated disease OPA1
Phenotype details -
Diagnosis/Initial optical atrophy
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Vision/Acuity -
Vision/Colour -
Vision/Field -
Birth_Details -
Eye/Optic_Disc -
Eye/OCT -
Brain/Imaging -
MotorSkills -
Vision/Abnormality -
Hearing/Loss -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-09-29 13:19:55 +02:00 (CEST)
Date last edited N/A

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