Disease #00457 (afibrinogenemia, congenital, OMIM:202400)

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	Curator: Johan T. den Dunnen

Official abbreviation	-
Name	afibrinogenemia, congenital
OMIM ID	202400
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	FGA, FGB, FGG
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-07-11 19:14:25 +02:00 (CEST)
Date last edited	N/A