FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term congenital afibrinogenemia ID (Ontology) DOID:2236 (Human Disease)
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).
Also Known As "Factor I deficiency" ; "Fibrinogen deficiency"
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 Genes
 congenital afibrinogenemia       4
 for disease ribbon | congenital afibrinogenemia       4
 model of | congenital afibrinogenemia       4
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
disease                          |
 |__physical disorder____________|
hematopoietic system disease     |
 |__blood coagulation disease____|
                                 congenital afibrinogenemia  4 rec.
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Is a autosomal recessive disease
physical disorder
blood coagulation disease
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Synonyms
  • "Factor I deficiency" EXACT
    "Fibrinogen deficiency" EXACT
Secondary IDs
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GARD:5761
MESH:D000347
MIM:202400
NCI:C98130
SNOMEDCT_US_2023_03_01:278504009
UMLS_CUI:C0001733