Phenotype #0000267828

Individual ID 00372513
Associated disease -
Phenotype details see paper; ...
Diagnosis/Initial Leber congenital amaurosis
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-05-08 09:43:10 +02:00 (CEST)
Date last edited N/A

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