Phenotype #0000057532

Individual ID 00077757
Associated disease STGD1
Phenotype details Stargardt disease; y29: Visual acuity 1.30/1.00 (OD/OS), central, atrophic appearing macular lesion with or without perifoveal flecks, normal ERG.
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 16y
Phenotype/Onset unknown
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2016-02-22 12:22:09 +01:00 (CET)
Date last edited N/A

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