OBO ID: DOID:2215
Term Name: factor VII deficiency Search Ontology:
Synonyms:
  • deficiency, stable
Definition: A blood coagulation disease that is characterized by easy bleeding, has_symptom epistaxis, bleeding of the gums, menorrhagia, and occasionally hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation in the F7 gene, which encodes coagulation factor VII, an important factor in the clotting cascade. (2)
References:
  • GARD:2238
  • ICD10CM:D68.2
  • MESH:D005168
  • NCI:C131631
  • SNOMEDCT_US_2023_03_01:154820003
  • UMLS_CUI:C0015503
Ontology: Human Disease   ( DOID:2215 )
Relationships
is a type of:
OTHER factor VII deficiency PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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