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439000005: Hyperfibrinogenemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2789153017 Hyperfibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2793786017 Hyperfibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2795467014 Hyperfibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperfibrinogenemia (disorder) Is a Fibrinogen abnormality true Inferred relationship Some
Hyperfibrinogenemia (disorder) Has definitional manifestation Fibrinogen in blood above reference range (finding) false Inferred relationship Some
Hyperfibrinogenemia (disorder) Has interpretation Above reference range true Inferred relationship Some 1
Hyperfibrinogenemia (disorder) Is a Fibrinogen in blood above reference range (finding) true Inferred relationship Some
Hyperfibrinogenemia (disorder) Interprets Fibrinogen measurement true Inferred relationship Some 1
Hyperfibrinogenemia (disorder) Interprets Hemostatic function true Inferred relationship Some 2
Hyperfibrinogenemia (disorder) Has interpretation Abnormal true Inferred relationship Some 2
Hyperfibrinogenemia (disorder) Interprets Fibrinogen assay, quantitative false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary hyperfibrinogenemia (disorder) Is a True Hyperfibrinogenemia (disorder) Inferred relationship Some

Reference Sets

GB English

US English

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