Phenotype #0000239426

Individual ID	00315680
Associated disease	WS
Diagnosis/Initial	Waardenburg syndrome
Diagnosis/Definite	WS1
Phenotype details	Some relatives show cutaneous depigmentations and/or early greying without dystopia canthorum and deafness; they do not carry the mutation
Inheritance	Isolated (sporadic)
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	Veronique Pingault
Database submission license	No license selected
Created by	Veronique Pingault
Date created	2009-10-05 13:39:46 +02:00 (CEST)
Date last edited	2010-02-04 14:28:03 +01:00 (CET)

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