FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.7.12 | FHIR Version n/a User: [n/a]

402853002: Cryofibrinogenemic purpura (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

1770777015 Cryofibrinogenemic purpura (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1781945010 Cryofibrinogenemic purpura en Synonym Active Entire term case insensitive SNOMED CT core module

1783770012 Purpura due to cryofibrinogenaemia en Synonym Active Entire term case insensitive SNOMED CT core module

1784156013 Purpura due to cryofibrinogenemia en Synonym Active Entire term case insensitive SNOMED CT core module

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cryofibrinogenemic purpura	Is a	Purpuric disorder	true	Inferred relationship	Existential restriction modifier
Cryofibrinogenemic purpura	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier
Cryofibrinogenemic purpura	Associated morphology	Purpura	false	Inferred relationship	Existential restriction modifier
Cryofibrinogenemic purpura	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Cryofibrinogenemic purpura	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Existential restriction modifier
Cryofibrinogenemic purpura	Has definitional manifestation	Purpura	false	Inferred relationship	Existential restriction modifier
Cryofibrinogenemic purpura	Associated morphology	Purpura	true	Inferred relationship	Existential restriction modifier	1
Cryofibrinogenemic purpura	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	1
Cryofibrinogenemic purpura	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier	2
Cryofibrinogenemic purpura	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
1770777015	Cryofibrinogenemic purpura (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1781945010	Cryofibrinogenemic purpura	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1783770012	Purpura due to cryofibrinogenaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1784156013	Purpura due to cryofibrinogenemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module