Phenotype #0000350984

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00465436
Associated disease	SNHL
Phenotype details	see paper; ..., profound sensorineural hearing loss
Diagnosis/Initial	auditory neuropathy spectrum disorder
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	DFNA6
Age/Examination	-
Age/Diagnosis	-
Age/Onset	00y03m
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2025-05-18 11:43:46 +02:00 (CEST)
Date last edited	N/A

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