Disease #04471 (Dysfibrinogenemia, congenital, OMIM:616004)

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	Curator: Johan T. den Dunnen

Official abbreviation	-
Name	Dysfibrinogenemia, congenital
OMIM ID	616004
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	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	N/A