"DOID:2236"^^ . _:vb50950647 . . "OMIM mapping confirmed by DO. [SN]."^^ . "disease_ontology"^^ . . "A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I)."^^ . _:vb50950648 . "congenital afibrinogenemia"^^ . "Factor I deficiency"@en . "UMLS_CUI:C0001733"^^ . _:vb50950647 . . . . "OMIM:202400"^^ . "GARD:5761"^^ . . "SNOMEDCT_US_2021_09_01:278504009"^^ . _:vb50950648 . "MESH:D000347"^^ . _:vb50950647 . _:vb50950648 . _:vb50950648 . "NCI:C98130"^^ . "Fibrinogen deficiency"@en . _:vb50950647 . _:vb50950648 . _:vb50950647 .