Phenotype #0000305678

Individual ID 00413713
Associated disease -
Phenotype details BCVA: 20/63; 20/32, HVF 258, Rods nondetectable; cones reduced by 97% and delayed
Diagnosis/Initial Possible autosomal dominant retinitis pigmentosa (adRP)
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 42y (42 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2022-07-22 03:34:11 +02:00 (CEST)
Date last edited N/A

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