24149006: Hemorrhagic disease of the newborn due to factor II deficiency (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Bleeding (finding)\Haemorrhage of newborn\Haemorrhagic disease of the newborn due to factor II deficiency

\Functional finding\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Acquired coagulation disorder\Neonatal coagulation disorder (disorder)\Haemorrhagic disease of the newborn due to factor II deficiency

\Finding of neonate\Neonatal disorder\...

\Neonatal coagulation disorder (disorder)\Haemorrhagic disease of the newborn due to factor II deficiency

\Haemorrhage of newborn\Haemorrhagic disease of the newborn due to factor II deficiency

\Disease\Disorder of foetus and/or newborn\Neonatal disorder\Neonatal coagulation disorder (disorder)\Haemorrhagic disease of the newborn due to factor II deficiency
\Disease\Disorder of foetus and/or newborn\Neonatal disorder\Haemorrhage of newborn\Haemorrhagic disease of the newborn due to factor II deficiency
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Acquired coagulation disorder\Neonatal coagulation disorder (disorder)\Haemorrhagic disease of the newborn due to factor II deficiency

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Haemorrhagic disease of the newborn due to factor II deficiency	Is a	Neonatal coagulation disorder (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Is a	Factor II deficiency (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Is a	Haemorrhage of newborn	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Occurrence	Neonatal	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Associated morphology	Hemorrhage	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Haemorrhagic disease of the newborn due to factor II deficiency	Occurrence	Perinatal state	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Occurrence	Fetal period (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Finding site	Fetal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Occurrence	période périnatale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Associated etiologic finding	Factor II deficiency (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Due to	Factor II deficiency (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Haemorrhagic disease of the newborn due to factor II deficiency	Occurrence	Neonatal	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Haemorrhagic disease of the newborn due to factor II deficiency	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Has definitional manifestation	Hemostatic system finding (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemorrhagic disease of the newborn due to factor II deficiency	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Haemorrhagic disease of the newborn due to factor II deficiency	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Haemorrhagic disease of the newborn due to factor II deficiency	Occurrence	Neonatal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
40543019	Hemorrhagic disease of the newborn due to factor II deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
40544013	Acquired neonatal factor II deficiency disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
481838014	Haemorrhagic disease of the newborn due to factor II deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
753752014	Hemorrhagic disease of the newborn due to factor II deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
40543019	Hemorrhagic disease of the newborn due to factor II deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
40544013	Acquired neonatal factor II deficiency disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
481838014	Haemorrhagic disease of the newborn due to factor II deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
753752014	Hemorrhagic disease of the newborn due to factor II deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6279881000241110	maladie hémorragique du nouveau-né due à un déficit en prothrombine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6279891000241112	maladie hémorragique du nouveau-né due à un déficit en facteur II de la coagulation	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6279881000241110	maladie hémorragique du nouveau-né due à un déficit en prothrombine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6279891000241112	maladie hémorragique du nouveau-né due à un déficit en facteur II de la coagulation	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module