Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	FG SYNDROME 2
Synonyms	FGS2
ID	http://purl.bioontology.org/ontology/OMIM/300321
altLabel	FGS2
cui	C1845902
Gene Locus	Xq28
Gene Symbol	FLN1 FLNA MNS CVD1 CSBS OPD2 NHBP FMD OPD1
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	300321
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	FG SYNDROME 2
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