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234456000: Congenital fibrinogen abnormality (disorder)

Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

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

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital fibrinogen abnormality Has interpretation Abnormal true Inferred relationship Some 2
Congenital fibrinogen abnormality Interprets Haemostatic function true Inferred relationship Some 2
Congenital fibrinogen abnormality Is a Congenital disease true Inferred relationship Some
Congenital fibrinogen abnormality Occurrence Congenital true Inferred relationship Some 1
Congenital fibrinogen abnormality Finding site Body system structure false Inferred relationship Some
Congenital fibrinogen abnormality Has definitional manifestation Haemostatic system finding false Inferred relationship Some
Congenital fibrinogen abnormality Is a Fibrinogen abnormality true Inferred relationship Some
Congenital fibrinogen abnormality Finding site Entire haematological system false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary factor I deficiency disease Is a True Congenital fibrinogen abnormality Inferred relationship Some
Hypofibrinogenaemia Is a False Congenital fibrinogen abnormality Inferred relationship Some
Hypodysfibrinogenaemia Is a True Congenital fibrinogen abnormality Inferred relationship Some
Dysfibrinogenaemia Is a True Congenital fibrinogen abnormality Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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