Visualize Submit Comment
Metadata
ID DOID:2236
Name congenital afibrinogenemia
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
Xrefs

GARD:5761

MESH:D000347

NCI:C98130

OMIM:202400

SNOMEDCT_US_2019_09_01:278504009

UMLS_CUI:C0001733

Subsets

NCIthesaurus

Synonyms

Factor I deficiency [EXACT]

Fibrinogen deficiency [EXACT]

Parent Relationships

is_a blood coagulation disease

is_a autosomal recessive disease

Add an item to the term tracker