Phenotype #0000144740

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	00184610
Associated disease	CCDS3;GATMD
Diagnosis/Initial	GAMT deficiency
Diagnosis/Definite	CCDS-3
Phenotype details	-
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Rahma MANI
Database submission license	No license selected
Created by	Gajja Salomons
Date created	2016-08-30 16:36:34 +02:00 (CEST)
Date last edited	N/A

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