Phenotype #0000216631

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	00282466
Associated disease	?
Diagnosis/Initial	Hearing impairment, non-syndromic, autosomal recessive
Diagnosis/Definite	-
Phenotype details	-
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Tumor/MSI	-
Diagnosis/Criteria	-
Owner name	Julia Lopez
Database submission license
Created by	Julia Lopez
Date created	2020-02-05 13:36:16 +01:00 (CET)
Date last edited	N/A

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