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234456000: Congenital fibrinogen abnormality (disorder)


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
110621000077110 anomalie congénitale du fibrinogène fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
351284017 Congenital fibrinogen abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
382291000077117 anomalie congénitale du fibrinogène (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
622778010 Congenital fibrinogen abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
anomalie congénitale du fibrinogène a pour interprétation (attribut) anormal true Inferred relationship Some 2
anomalie congénitale du fibrinogène interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 2
anomalie congénitale du fibrinogène est un(e) (attribut) Congenital disease true Inferred relationship Some
anomalie congénitale du fibrinogène survenue (attribut) congénital true Inferred relationship Some 1
anomalie congénitale du fibrinogène localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
anomalie congénitale du fibrinogène est défini par la manifestation de (attribut) constatation sur le système hémostatique false Inferred relationship Some
anomalie congénitale du fibrinogène est un(e) (attribut) Fibrinogen abnormality true Inferred relationship Some
anomalie congénitale du fibrinogène localisation d'une constatation (attribut) Entire hematological system (body structure) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary factor I deficiency disease est un(e) (attribut) True anomalie congénitale du fibrinogène Inferred relationship Some
Hypofibrinogenaemia est un(e) (attribut) False anomalie congénitale du fibrinogène Inferred relationship Some
Hypodysfibrinogenaemia est un(e) (attribut) True anomalie congénitale du fibrinogène Inferred relationship Some
Dysfibrinogenemia est un(e) (attribut) True anomalie congénitale du fibrinogène Inferred relationship Some

This concept is not in any reference sets

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