Phenotype #0000127749

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00155199
Associated disease	CPDX2
Phenotype details	severe foetal form
Diagnosis/Initial	chondrodysplasia punctata
Inheritance	Familial, X-linked dominant
Diagnosis/Definite	CDPX-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	2018-03-13 16:10:37 +01:00 (CET)
Date last edited	2018-03-15 15:42:01 +01:00 (CET)

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