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Disease Ontology Browser
congenital afibrinogenemia (DOID:2236)
Synonyms: Factor I deficiency; Fibrinogen deficiency
Alt IDs: OMIM:202400, ICD10CM:D68.2, MESH:D000347, NCI:C26692, NCI:C98130, UMLS_CUI:C0001733

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/12/2017
MGI 6.10
The Jackson Laboratory