Phenotype #0000301655

Individual ID 00409538
Associated disease MOPD1
Phenotype details best corrected visual acuity: 1.2; electroretinogram , rod: mildly reduced, cone: mildly reduced
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite dystrophy, corneoretinal, crystalline, Bietti (BCD)
Age/Examination 60y (60 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 2022-05-10 12:05:14 +02:00 (CEST)
Date last edited N/A

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