Phenotype #0000254268

Individual ID 00358970
Associated disease retinal disease
Phenotype details see paper; ...
Diagnosis/Initial Leber Congenital Amaurosis
Inheritance Familial, autosomal recessive
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