Phenotype #0000310608

Individual ID 00419322
Associated disease -
Phenotype details phenotype: unaffected; diagnosis in affected male relatives: retinitis pigmentosa
Diagnosis/Initial -
Inheritance Familial, X-linked
Diagnosis/Definite retinitis pigmentosa
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 2022-10-19 19:08:27 +02:00 (CEST)
Date last edited N/A

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