congenital afibrinogenemia

Term ID

DOID:2236

Synonyms

• Factor I deficiency
• Fibrinogen deficiency

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). https://ghr.nlm.nih.gov/condition/congenital-afibrinogenemia#synonyms

References

• GARD:5761
• MESH:D000347
• NCI:C98130
• OMIM:202400
• SNOMEDCT_US_2023_03_01:278504009
• UMLS_CUI:C0001733

Ontology

Human Disease   ( DOID:2236 )