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Summary Literature (0)
MIM:616004 - DYSFIBRINOGENEMIA, CONGENITAL

Xenbase Genes: fga, fgb, fgg

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014452 - familial dysfibrinogenemia
MONDO:0016638 - familial hypodysfibrinogenemia
MONDO:0018060 - congenital fibrinogen deficiency