Phenotype #0000143729

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	00182967
Associated disease	deafness
Phenotype details	deafness (profound)
Diagnosis/Initial	non-syndromic deafness
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Viviana Karina Dalamón
Database submission license
Created by	Johan den Dunnen
Date created	2018-10-12 13:45:12 +02:00 (CEST)
Date last edited	N/A

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