Phenotype #0000085477

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00107712
Associated disease	MCLMR
Inheritance	Familial, autosomal recessive
Phenotype details	Non-syndromic hearing loss
Diagnosis/Initial	-
Age/Examination	-
Diagnosis/Definite	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Wenjun Xia
Database submission license	No license selected
Created by	Wenjun Xia
Date created	2017-06-22 03:40:56 +02:00 (CEST)
Date last edited	2017-07-17 09:35:15 +02:00 (CEST)

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