Phenotype #0000301105

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00408987
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
Created by	Anna Tracewska
Date created	2022-04-29 17:32:37 +02:00 (CEST)
Date last edited	N/A

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