Phenotype #0000092590

Individual ID 00117355
Associated disease STL1
Phenotype details severe myopia, bilateral
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset mbarat-houari
Protein -
Owner name Mouna Barat-Houari
Database submission license No license selected
Created by Mouna Barat-Houari
Date created 2017-08-21 16:09:47 +02:00 (CEST)
Date last edited 2017-08-21 16:12:58 +02:00 (CEST)

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