Phenotype #0000090512

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	00115030
Associated disease	CHTE
Phenotype details	IGSF1 deficiency syndrome; OMIM300888
Diagnosis/Initial	-
Inheritance	Familial, X-linked recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Yu Sun
Database submission license	No license selected
Created by	Yu Sun
Date created	2013-08-30 15:07:25 +02:00 (CEST)
Date last edited	2017-08-07 14:21:52 +02:00 (CEST)

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