Phenotype #0000092560

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	00043769
Associated disease	KDVS
Phenotype details	17q21.31 deletion syndrome, see paper; …
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	12m
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	David Koolen
Database submission license	No license selected
Created by	David Koolen
Date created	2015-06-19 13:33:28 +02:00 (CEST)
Date last edited	N/A

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