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Summary Literature (0)
MIM:202400 - AFIBRINOGENEMIA, CONGENITAL

Xenbase Genes: fgg, fga, fgb

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008737 - congenital afibrinogenemia
MONDO:0015096 - familial hypofibrinogenemia
MONDO:0018060 - congenital fibrinogen deficiency

Disease Ontology (DO):
DOID:2236 - congenital afibrinogenemia