FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.8.2 | FHIR Version n/a User: [n/a]

76407009: Protein C deficiency disease (disorder)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1233987014 Protein C deficiency en Synonym Active Initial character case insensitive SNOMED CT core

126889016 Protein C deficiency disease en Synonym Active Initial character case insensitive SNOMED CT core

817124014 Protein C deficiency disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Protein C deficiency disease	Interprets	Haemostatic function	true	Inferred relationship	Some	1
Protein C deficiency disease	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Protein C deficiency disease	Is a	Thrombophilia	true	Inferred relationship	Some
Protein C deficiency disease	Is a	Deficiency of naturally occurring coagulation factor inhibitor	true	Inferred relationship	Some
Protein C deficiency disease	Finding site	Body system structure	false	Inferred relationship	Some
Protein C deficiency disease	Has definitional manifestation	Haemostatic system finding	false	Inferred relationship	Some
Protein C deficiency disease	Finding site	Entire haematological system	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Acquired protein C deficiency	Is a	True	Protein C deficiency disease	Inferred relationship	Some
Hereditary protein C deficiency	Is a	True	Protein C deficiency disease	Inferred relationship	Some
Thrombophilia due to acquired protein C deficiency	Is a	False	Protein C deficiency disease	Inferred relationship	Some
Family history of protein C deficiency	Associated finding	True	Protein C deficiency disease	Inferred relationship	Some	1
Thrombophilia due to acquired protein C deficiency	Due to	False	Protein C deficiency disease	Inferred relationship	Some	1

Reference Sets

Australian emergency department reference set

Id	Description	Lang	Type	Status	Case?	Module
1233987014	Protein C deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
126889016	Protein C deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
817124014	Protein C deficiency disease (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core