76642003: Factor X deficiency (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\...

\Prothrombin complex deficiency\Factor X deficiency

\Coagulation factor deficiency syndrome\Factor X deficiency

\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\...

\Prothrombin complex deficiency\Factor X deficiency

\Coagulation factor deficiency syndrome\Factor X deficiency

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

127274011 Factor X deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

817385017 Factor X deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1234012018 Stuart-Prower factor deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3036019012 Factor 10 deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

127274011 Factor X deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

127274011 Factor X deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

817385017 Factor X deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

817385017 Factor X deficiency (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

817385017 Factor X deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1234012018 Stuart-Prower factor deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1234012018 Stuart-Prower factor deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3036019012 Factor 10 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3036019012 Factor 10 deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3390011001000116 Faktor X-Mangel, kongenitaler de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4640331000241119 déficit en facteur X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4640331000241119 déficit en facteur X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3390011001000116 Faktor X-Mangel, kongenitaler de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Factor X deficiency	Is a	Prothrombin complex deficiency	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor X deficiency	Is a	Coagulation factor deficiency syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor X deficiency	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor X deficiency	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor X deficiency	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor X deficiency	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Factor X deficiency	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Acquired factor X deficiency disease (disorder)	Is a	True	Factor X deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary factor X deficiency disease	Is a	True	Factor X deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)
Deficiency of factor X due to systemic amyloidosis (disorder)	Is a	True	Factor X deficiency	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

Description inactivation indicator reference set