Phenotype #0000285583

Individual ID 00392307
Associated disease -
Phenotype details clinical signs of RP without symptoms, electroretinography: responses reduced and delayed
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite retinitis pigmentosa
Age/Examination 60y (60 years)
Age/Diagnosis 58y
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 2021-11-22 13:18:51 +01:00 (CET)
Date last edited N/A

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