Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	FG SYNDROME 3
Synonyms	FGS3
ID	http://purl.bioontology.org/ontology/OMIM/300406
altLabel	FGS3
cui	C1845567
Gene Locus	Xp22.3
Gene Symbol	FGS3
MIMTYPEMEANING	Mendelian phenotype or locus, molecular basis unknown.
notation	300406
OMIM Entry Type	5
OMIM MimType Value	perc
prefLabel	FG SYNDROME 3
tui	T047

Delete	Subject	Author	Type	Created
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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/C537923	Medical Subject Headings	CUI