has material basis in germline mutation in F13B factor XIII, b subunit, deficiency of https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/factor_xiii_b_subunit_deficiency_of OMIM:613235 GARD:0015635 factor XIII, b subunit, deficiency of MEDGEN:442490 UMLS:C2750481 MONDO:0013190 factor XIIIB deficiency MESH:C567688 congenital factor XIII deficiency inherited blood coagulation disorder