Global Variome shared LOVD

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Phenotype #0000298542 Individual ID 00406043 Associated disease - Phenotype details Non-Nystagmus; Convergent strabismus; Hearing loss; Myopia; Glaucoma; Tubular visual field; Nyctalopia Diagnosis/Initial retinitis pigmentosa (RP) Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 47y (47 years) Age/Diagnosis - Age/Onset 10y-19y Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-03-25 07:05:25 +01:00 (CET) Date last edited N/A

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