Phenotype #0000105073

Individual ID	00132290
Associated disease	DFNB;ARNSHL
Phenotype details	autosomal recessive bilateral nonsyndromic hearing loss with vestibular dysfunction (symmetric, sensorineural, likely congenital, progressing from severe to profound); patients did not develop normal speech, delayed motor development; electronystagmography in caloric and rotary testing shows impaired vestibular function
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Jacopo Celli
Date created	2010-07-22 11:33:16 +02:00 (CEST)
Date last edited	2017-10-25 22:41:08 +02:00 (CEST)

Global Variome shared LOVD