Phenotype #0000272681

Individual ID 00377531
Associated disease -
Phenotype details see paper
Diagnosis/Initial retinal disease
Inheritance Isolated (sporadic)
Diagnosis/Definite Leber congenital amaurosis
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-07-22 15:35:32 +02:00 (CEST)
Date last edited N/A

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