Phenotype #0000284369

Individual ID 00390881
Associated disease retinal disease
Phenotype details -
Diagnosis/Initial Leber congenital amaurosis (LCA)
Inheritance Unknown
Diagnosis/Definite -
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 Julia Lopez

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