Phenotype #0000273052

Individual ID 00377906
Associated disease retinal disease
Phenotype details poor vision; photophobia; NYS
Diagnosis/Initial Leber Congenital Amaurosis
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 3y2m (3 years, 2 months)
Age/Diagnosis -
Age/Onset <1y
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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