Phenotype #0000241766

Individual ID 00317982
Associated disease OPA1
Phenotype details Optic atrophy, positive family history, suspicion of AD inheritance
Diagnosis/Initial -
Inheritance Unknown
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 Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2020-11-05 14:16:23 +01:00 (CET)
Date last edited 2020-11-11 14:44:38 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.