Global Variome shared LOVD

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Phenotype #0000301104 Individual ID 00408986 Associated disease USH3B Inheritance Familial, autosomal recessive Phenotype details retinitis pigmentosa; progressive sensorineural hearing loss; episodic psychosis Diagnosis/Initial - Age/Examination - Diagnosis/Definite Usher syndrome, type 3B (USH-3B) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-04-29 17:32:37 +02:00 (CEST) Date last edited N/A

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