33169001: Factor XI deficiency, type II (disorder)

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

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\...

\Contact factor deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type II

\Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor XI deficiency disease\Factor XI deficiency, type II

\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Contact factor deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type II
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor XI deficiency disease\Factor XI deficiency, type II

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

55354017 Factor XI deficiency, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

764538019 Factor XI deficiency, type II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Factor XI deficiency, type II	Is a	Hereditary factor XI deficiency disease	true	Inferred relationship	Some
Factor XI deficiency, type II	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Factor XI deficiency, type II	Finding site	Body system structure	false	Inferred relationship	Some
Factor XI deficiency, type II	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Factor XI deficiency, type II	Occurrence	Congenital	true	Inferred relationship	Some	2
Factor XI deficiency, type II	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Factor XI deficiency, type II	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

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This concept is not in any reference sets