Disease #00202 (SGS (Shprintzen-Goldberg craniosynostosis syndrome (SGS)), OMIM:182212)

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	Curator: Johan T. den Dunnen

Official abbreviation	SGS
Name	Shprintzen-Goldberg craniosynostosis syndrome (SGS)
OMIM ID	182212
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SKI
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-09-17 22:48:52 +02:00 (CEST)
Date last edited	N/A