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Disease Ontology Browser
congenital afibrinogenemia (DOID:2236)
Alliance: disease page
Synonyms: Factor I deficiency; Fibrinogen deficiency
Alt IDs: OMIM:202400, MESH:D000347, NCI:C98130, UMLS_CUI:C0001733
Definition: 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).

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.21
The Jackson Laboratory