Phenotype #0000239287

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	00315542
Associated disease	WS
Diagnosis/Initial	Waardenburg syndrome
Diagnosis/Definite	WS4
Phenotype details	depigmentation in father
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	Veronique Pingault
Database submission license	No license selected
Created by	Veronique Pingault
Date created	2009-11-18 15:30:08 +01:00 (CET)
Date last edited	2010-02-04 15:18:07 +01:00 (CET)

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