OBO ID: DOID:2236
Term Name: congenital afibrinogenemia Search Ontology:
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)
OTHER congenital afibrinogenemia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FGA Afibrinogenemia, congenital 202400
FGB Hypofibrinogenemia, congenital 202400
Afibrinogenemia, congenital 202400
FGG Afibrinogenemia, congenital 202400
Hypofibrinogenemia, congenital 202400
PHENOTYPE No data available

CITATIONS (3)