FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

439000005: Hyperfibrinogenemia (disorder)

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

Descriptions:

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

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperfibrinogenemia Is a Fibrinogen abnormality true Inferred relationship Existential restriction modifier
Hyperfibrinogenemia Has definitional manifestation Fibrinogen in blood above reference range false Inferred relationship Existential restriction modifier
Hyperfibrinogenemia Has interpretation Above reference range true Inferred relationship Existential restriction modifier 1
Hyperfibrinogenemia Is a Fibrinogen in blood above reference range true Inferred relationship Existential restriction modifier
Hyperfibrinogenemia Interprets Fibrinogen measurement true Inferred relationship Existential restriction modifier 1
Hyperfibrinogenemia Interprets Hemostatic function true Inferred relationship Existential restriction modifier 2
Hyperfibrinogenemia Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Hyperfibrinogenemia Interprets Fibrinogen assay, quantitative false Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary hyperfibrinogenemia Is a True Hyperfibrinogenemia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start