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234456000: congenitale afwijking van fibrinogeen (aandoening)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
351284017 Congenital fibrinogen abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622778010 Congenital fibrinogen abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6667711000146113 congenitale afwijking van fibrinogeen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6667721000146115 congenitale afwijking van fibrinogeen (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6667731000146118 congenitale afwijking van stollingsfactor I nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital fibrinogen abnormality Is a Fibrinogen abnormality true Inferred relationship Some
Congenital fibrinogen abnormality Finding site Entire hematological system (body structure) false Inferred relationship Some
Congenital fibrinogen abnormality Is a Congenital disease (disorder) true Inferred relationship Some
Congenital fibrinogen abnormality Occurrence Congenital true Inferred relationship Some 1
Congenital fibrinogen abnormality Finding site Body system structure false Inferred relationship Some
Congenital fibrinogen abnormality Has definitional manifestation Hemostatic system finding false Inferred relationship Some
Congenital fibrinogen abnormality Has interpretation Abnormal true Inferred relationship Some 2
Congenital fibrinogen abnormality Interprets Hemostatic function true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Hypofibrinogenaemia Is a False Congenital fibrinogen abnormality Inferred relationship Some
Hypodysfibrinogenaemia Is a True Congenital fibrinogen abnormality Inferred relationship Some
Dysfibrinogenemia Is a True Congenital fibrinogen abnormality Inferred relationship Some
Hereditary factor I deficiency disease Is a True Congenital fibrinogen abnormality Inferred relationship Some

This concept is not in any reference sets

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