Search Ontology:
Human Disease

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
Ontology
Human Disease   ( DOID:2236 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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