Phenotype #0000052029

Individual ID 00072359
Associated disease OPA
Phenotype details Ataxia, Myopathy
Diagnosis/Initial -
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 Tonino Ercolino
Database submission license No license selected
Created by Tonino Ercolino
Date created 2005-01-24 14:55:25 +01:00 (CET)
Date last edited 2006-03-24 10:09:39 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.