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DO Term : thrombophilia due to activated protein C resistance [DOID:0111902] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A thrombophilia characterized by resistance of F5 to cleavage and inactivation and increased tendency for thrombosis that has_material_basis_in heterozygous mutation in F5 on chromosome 1q24.2.

synonyms:
OMIM:188055,
UMLS_CUI:C1861171,
thrombophilia due to deficiency of activated protein C cofactor,
PCCF deficiency,
APC resistance,
thrombophilia V,
THPH2,
activated protein C resistance,
188055,
PROC cofactor deficiency,
MESH:C566056

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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