Phenotype #0000286005

Individual ID 00392758
Associated disease STGD1
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 16y (16 years)
Age/Diagnosis 16y
Age/Onset 14y
Phenotype/Onset Impaired vision
Protein -
Owner name Lu Tian
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Lu Tian
Date created 2021-11-24 02:06:07 +01:00 (CET)
Date last edited 2021-11-26 11:37:18 +01:00 (CET)

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