Phenotype #0000295598

Individual ID 00402837
Associated disease -
Phenotype details lesions, right eye/left eye: single, vitelliruptive lesion/vitelliruptive lesion, visual acuity: right eye, left eye: 20/100, 20/63, color vision: errors, visual field: relative scotoma, electro-oculogram right eye/left eye: 149/141
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite dystrophy, macular, vitelliform type 2 (VMD2)
Age/Examination 56y5m (56 years, 5 months)
Age/Diagnosis -
Age/Onset 21y
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-02-11 14:52:14 +01:00 (CET)
Date last edited N/A

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