Phenotype #0000298825

Individual ID 00406338
Associated disease -
Phenotype details photoaversion, best corrected visual acuity right, left eye: 2/60, 3/60, refractive error: none, colour vision - Ishihara: 0/17, fundus: perifoveal retinal thinning
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite cone dystrophy
Age/Examination 44y (44 years)
Age/Diagnosis -
Age/Onset 23y
Phenotype/Onset reduced central vision
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-03-28 19:16:38 +02:00 (CEST)
Date last edited N/A

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