Phenotype #0000188531

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00249649
Associated disease	CDG1C
Phenotype details	growth retardation, hypotonia, cataracts, enlarged spleen, poor feeding, no cerebellar hypoplasia, normal liver function test
Diagnosis/Initial	-
Inheritance	-
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Gert Matthijs
Database submission license	No license selected
Created by	Gert Matthijs
Date created	2012-09-02 12:01:45 +02:00 (CEST)
Date last edited	2013-01-10 15:47:02 +01:00 (CET)

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