Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	AFIBRINOGENEMIA, CONGENITAL
Synonyms	HYPOFIBRINOGENEMIA, CONGENITAL
ID	http://purl.bioontology.org/ontology/OMIM/202400
altLabel	HYPOFIBRINOGENEMIA, CONGENITAL
cui	C2584774
Gene Locus	4q28
Gene Symbol	FGG
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	202400
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	AFIBRINOGENEMIA, CONGENITAL
tui	T047

Delete	Subject	Author	Type	Created
No notes to display

Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/D000347	Medical Subject Headings	CUI
	http://purl.bioontology.org/ontology/ICD10CM/D68.2	International Classification of Diseases, Version 10 - Clinical Modification	CUI