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439698008: Hereditary thrombophilia (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
2789416017 Hereditary thrombophilia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2794141016 Hereditary thrombophilia en Synonym Active Entire term case insensitive SNOMED CT core module
2794142011 Hereditary hypercoagulable disorder en Synonym Active Entire term case insensitive SNOMED CT core module
2871986010 Primary thrombophilia en Synonym Active Entire term case insensitive SNOMED CT core module

23 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary thrombophilia Is a Thrombophilia true Inferred relationship Existential restriction modifier
Hereditary thrombophilia Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hereditary thrombophilia Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Hereditary thrombophilia Is a Hereditary disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary antithrombin III deficiency Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Hereditary heparin cofactor II deficiency Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Hereditary protein S deficiency Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Hereditary protein C deficiency Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Hereditary hyperfibrinogenemia Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Hereditary hyperhomocysteinemia Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Hereditary thrombophilic dysfibrinogenemia Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Prothrombin G20210A mutation Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Hereditary elevated factor XI Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Hereditary elevated factor VIII Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Factor V Leiden mutation Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier
Resistance to activated protein C caused by Factor V Leiden Is a True Hereditary thrombophilia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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