Disease #00769 (FGS-4 (FG syndrome, type 4 (FGS-4)), OMIM:300422)

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	Curator: Johan T. den Dunnen

Official abbreviation	FGS-4
Name	FG syndrome, type 4 (FGS-4)
OMIM ID	300422
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CASK
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A