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Metadata
ID	DOID:0112174
Name	combined deficiency of vitamin K-dependent clotting factors 2
Definition	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. https://pubmed.ncbi.nlm.nih.gov/14765194/
Xrefs	MESH:C564393 MIM:607473
Synonyms	VKCFD2 [EXACT]
Parent Relationships	is_a hereditary combined deficiency of vitamin K-dependent clotting factors is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance