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Summary Literature (0)
MIM:613235 - FACTOR XIII, B SUBUNIT, DEFICIENCY OF

Xenbase Genes: f13b, f13bl

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013190 - factor XIII, b subunit, deficiency of
MONDO:0018029 - congenital factor XIII deficiency

Disease Ontology (DO):
DOID:2211 - factor XIII deficiency