Search Ontology:
Human Disease

factor VII deficiency

Term ID
DOID:2215
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
  • MIM:227500
  • NCI:C131631
  • ORDO:327
  • SNOMEDCT_US_2023_03_01:154820003
  • UMLS_CUI:C0015503
Ontology
Human Disease   ( DOID:2215 )
Relationships
is a type of
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Genes Involved
Zebrafish Models