Phenotype #0000285793

Individual ID 00392536
Associated disease STGD1
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 15y (15 years)
Age/Diagnosis 15y
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 2021-11-23 09:29:48 +01:00 (CET)
Date last edited 2021-11-26 11:37:18 +01:00 (CET)

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