88540000: Factor XI deficiency, type I (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.\...

\Contact factor deficiency (disorder)\Hereditary factor XI deficiency disease\Factor XI deficiency, type I

\Coagulation factor deficiency syndrome\Factor XI deficiency (disorder)\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
\Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor XI deficiency disease\Factor XI deficiency, type I

\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Contact factor deficiency (disorder)\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Factor XI deficiency (disorder)\Hereditary factor XI deficiency disease\Factor XI deficiency, type I
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor XI deficiency disease\Factor XI deficiency, type I

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

146804016 Factor XI deficiency, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

831245011 Factor XI deficiency, type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

146804016 Factor XI deficiency, type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

146804016 Factor XI deficiency, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

831245011 Factor XI deficiency, type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

831245011 Factor XI deficiency, type I (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

831245011 Factor XI deficiency, type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

6936451000241112 déficit en facteur XI de type I fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6936451000241112 déficit en facteur XI de type I fr 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 XI deficiency, type I	Is a	Hereditary factor XI deficiency disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor XI deficiency, type I	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor XI deficiency, type I	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor XI deficiency, type I	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Factor XI deficiency, type I	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Factor XI deficiency, type I	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Factor XI deficiency, type I	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

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This concept is not in any reference sets