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


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

In Mondo Disease Ontology:
MONDO:0008737 - congenital afibrinogenemia

Human Disease Resources: OMIM

Xenbase Genes: fga, fgb, fgg