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111589005: Dysfibrinogenemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
178844010 Dysfibrinogenemia en Synonym Active Entire term case insensitive SNOMED CT core module
363901010 Dysfibrinogenaemia en Synonym Active Entire term case insensitive SNOMED CT core module
632834017 Dysfibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dysfibrinogenemia Is a Congenital fibrinogen abnormality true Inferred relationship Existential restriction modifier
Dysfibrinogenemia Is a Coagulation factor deficiency syndrome false Inferred relationship Existential restriction modifier
Dysfibrinogenemia Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Dysfibrinogenemia Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Dysfibrinogenemia Finding site Body system structure false Inferred relationship Existential restriction modifier
Dysfibrinogenemia Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Dysfibrinogenemia Is a Factor I deficiency disease true Inferred relationship Existential restriction modifier
Dysfibrinogenemia Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Dysfibrinogenemia Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Alpha chain defect dysfibrinogenemia Is a True Dysfibrinogenemia Inferred relationship Existential restriction modifier
Beta chain defect dysfibrinogenemia Is a True Dysfibrinogenemia Inferred relationship Existential restriction modifier
Gamma chain defect dysfibrinogenemia Is a True Dysfibrinogenemia Inferred relationship Existential restriction modifier
Hereditary dysfibrinogenemia Is a True Dysfibrinogenemia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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