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Hereditary factor I deficiency disease

MedGen UID:: 9230
•Concept ID:: C0019250
•: Disease or Syndrome

Synonyms:	FGA-Related Congenital Afibrinogenemia; FGB-Related Congenital Afibrinogenemia; FGG-Related Congenital Afibrinogenemia
SNOMED CT:	Hereditary factor I deficiency disease (31925001); Hereditary hypofibrinogenemia (31925001)

Related genes: Gene(s) associated with related conditions. For conditions in a hierarchy, the parent condition will list the genes associated with the children conditions.	FGG, FGB, FGA

Definition

An inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVHereditary factor I deficiency disease

Phenotypic abnormality
- Abnormality of blood and blood-forming tissues
  - Abnormality of coagulation
    - Abnormality of the coagulation cascade
      - Coagulation factor deficiency syndrome
        Fibrinogen deficiency
        Hereditary factor I deficiency disease
        Afibrinogenemia
        Congenital afibrinogenemia
        Dysfibrinogenemia
        Familial hypodysfibrinogenemia

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