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DO Term : combined deficiency of vitamin K-dependent clotting factors 2 [DOID:0112174] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary combined deficiency of vitamin K-dependent clotting factors that has_material_basis_in homozygous or compound heterozygous mutation in the VKORC1 gene on chromosome 16p11.2.
  • synonyms:
  • OMIM:607473,
  • MESH:C564393,
  • VKCFD2,
  • 607473
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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