Disease #00052 (BGS (Baller-Gerold syndrome (BGS)), OMIM:218600)

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	Curator: Johan T. den Dunnen

Official abbreviation	BGS
Name	Baller-Gerold syndrome (BGS)
OMIM ID	218600
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RECQL4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-08-31 10:06:44 +02:00 (CEST)
Date last edited	N/A