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234456000: Congenital fibrinogen abnormality (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
351284017 Congenital fibrinogen abnormality en Synonym Active Entire term case insensitive SNOMED CT core module
622778010 Congenital fibrinogen abnormality (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital fibrinogen abnormality Is a Fibrinogen abnormality true Inferred relationship Existential restriction modifier
Congenital fibrinogen abnormality Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Congenital fibrinogen abnormality Is a Congenital disease true Inferred relationship Existential restriction modifier
Congenital fibrinogen abnormality Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital fibrinogen abnormality Finding site Body system structure false Inferred relationship Existential restriction modifier
Congenital fibrinogen abnormality Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Congenital fibrinogen abnormality Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Congenital fibrinogen abnormality Interprets Hemostatic function true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Hypofibrinogenemia Is a False Congenital fibrinogen abnormality Inferred relationship Existential restriction modifier
Hypodysfibrinogenemia Is a True Congenital fibrinogen abnormality Inferred relationship Existential restriction modifier
Dysfibrinogenemia Is a True Congenital fibrinogen abnormality Inferred relationship Existential restriction modifier
Hereditary factor I deficiency disease Is a True Congenital fibrinogen abnormality Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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