Disease #00388 (KBGS (KBG syndrome (KBGS)), OMIM:148050)

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	Curator: Johan T. den Dunnen

Official abbreviation	KBGS
Name	KBG syndrome (KBGS)
OMIM ID	148050
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ANKRD11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-05-29 10:09:45 +02:00 (CEST)
Date last edited	N/A