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33169001: stollingsfactor XI-deficiëntie type II (aandoening)

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:

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

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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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
6217281000146113	factor XI-deficiëntie type II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6217311000146111	PTA-deficiëntie type II	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6217331000146116	Rosenthal-syndroom type II	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6217361000146113	deficiëntie van plasmatromboplastineantecedent type II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6217381000146117	hemofilie C type II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9890811000146119	stollingsfactor XI-deficiëntie type II (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9892711000146110	stollingsfactor XI-deficiëntie type II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)