Disease #00773 (SGBS-1 (Simpson-Golabi-Behmel syndrome, type 1 (SGBS-1)), OMIM:312870)

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	Curator: Johan T. den Dunnen

Official abbreviation	SGBS-1
Name	Simpson-Golabi-Behmel syndrome, type 1 (SGBS-1)
OMIM ID	312870
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	GPC3, GPC4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A