Search Ontology:
Human Disease
factor VII deficiency
- Term ID
- DOID:2215
- Synonyms
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- 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
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- 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 )
- is a type of
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