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 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-04-29 17:32:37 +02:00 (CEST)
Date last edited N/A

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