FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term factor VII deficiency ID (Ontology) DOID:2215 (Human Disease)
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.
Also Known As "deficiency, stable"
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 Genes
 factor VII deficiency       1
 for disease ribbon | factor VII deficiency       1
 model of | factor VII deficiency       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
hematopoietic system disease     |
 |__blood coagulation disease____|
                                 factor VII deficiency  1 rec.
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Is a autosomal recessive disease
blood coagulation disease
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Synonyms
  • "deficiency, stable" EXACT
Secondary IDs
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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