Phenotype #0000128932

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	00163812
Associated disease	CPDX2
Phenotype details	severe fetal form
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	CPDX-2
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Fabienne Dufernez
Database submission license	No license selected
Created by	Fabienne Dufernez
Date created	2018-04-12 17:37:25 +02:00 (CEST)
Date last edited	N/A

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