Phenotype #0000304908

Individual ID 00412922
Associated disease -
Phenotype details spherical equivalent: -3.25/-3.25
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite retinitis pigmentosa associated with myopia
Age/Examination -
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 2022-07-06 16:27:41 +02:00 (CEST)
Date last edited N/A

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