Phenotype #0000286002

Individual ID 00392755
Associated disease STGD1
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 10y (10 years)
Age/Diagnosis 10y
Age/Onset 08y
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 01:45:57 +01:00 (CET)
Date last edited 2021-11-26 11:37:18 +01:00 (CET)

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