Phenotype #0000302047

Individual ID 00409933
Associated disease -
Phenotype details nyctalopia in infancy; visual field loss: 2nd decade of life; visual acuity loss: 2nd/3rd decade of life; best corrected visual acuity: counting fingers; macula: sheen, retinal pigment epithelium atrophic alterations
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite retinal dystrophy
Age/Examination 49y (49 years)
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 2022-05-14 11:49:20 +02:00 (CEST)
Date last edited N/A

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