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439698008: thrombophilie héréditaire (trouble)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2789416017 Hereditary thrombophilia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2794141016 Hereditary thrombophilia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2794142011 Hereditary hypercoagulable disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2871986010 Primary thrombophilia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
383401000172114 thrombophilie héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
709001000241114 thrombophilie héréditaire (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


23 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary thrombophilia (disorder) interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 1
Hereditary thrombophilia (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 1
Hereditary thrombophilia (disorder) est un(e) (attribut) maladie héréditaire true Inferred relationship Some
Hereditary thrombophilia (disorder) est un(e) (attribut) thrombophilie true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
résistance à la protéine C activée causée par le facteur V Leiden est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Hereditary antithrombin III deficiency (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Hereditary heparin cofactor II deficiency (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Hereditary protein S deficiency (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Hereditary protein C deficiency (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Hereditary hyperfibrinogenemia (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Hereditary hyperhomocysteinemia (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Hereditary thrombophilic dysfibrinogenemia (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Prothrombin G20210A mutation (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Hereditary elevated factor XI (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Hereditary elevated factor VIII (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
mutation du facteur V de Leiden est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder) est un(e) (attribut) True Hereditary thrombophilia (disorder) Inferred relationship Some

This concept is not in any reference sets

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