28293008: carence héréditaire en facteur VIII (trouble)

SNOMED CT Concept\constatation clinique\...

\constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...

\Factor VIII deficiency\Hereditary factor VIII deficiency disease (disorder)

\Hemophilia\Hereditary factor VIII deficiency disease (disorder)

\Hereditary coagulation factor deficiency\Hereditary factor VIII deficiency disease (disorder)

\Disease\Genetic disease\maladie héréditaire\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor VIII deficiency disease (disorder)
\Disease\Genetic disease\maladie héréditaire\Hereditary coagulation factor deficiency\Hereditary factor VIII deficiency disease (disorder)
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor VIII deficiency\Hereditary factor VIII deficiency disease (disorder)
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor VIII deficiency disease (disorder)
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor VIII deficiency disease (disorder)

Status: current, Not 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
Hereditary factor VIII deficiency disease (disorder)	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Hereditary factor VIII deficiency disease (disorder)	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Hereditary factor VIII deficiency disease (disorder)	est un(e) (attribut)	X-linked hereditary disease	true	Inferred relationship	Some
Hereditary factor VIII deficiency disease (disorder)	est un(e) (attribut)	Hemophilia	true	Inferred relationship	Some
Hereditary factor VIII deficiency disease (disorder)	est un(e) (attribut)	Hereditary coagulation factor deficiency	true	Inferred relationship	Some
Hereditary factor VIII deficiency disease (disorder)	est un(e) (attribut)	Factor VIII deficiency	true	Inferred relationship	Some
Hereditary factor VIII deficiency disease (disorder)	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Hereditary factor VIII deficiency disease (disorder)	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Hereditary factor VIII deficiency disease (disorder)	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Severe hereditary factor VIII deficiency disease (disorder)	est un(e) (attribut)	True	Hereditary factor VIII deficiency disease (disorder)	Inferred relationship	Some
Mild hereditary factor VIII deficiency disease (disorder)	est un(e) (attribut)	True	Hereditary factor VIII deficiency disease (disorder)	Inferred relationship	Some
Moderate hereditary factor VIII deficiency disease (disorder)	est un(e) (attribut)	True	Hereditary factor VIII deficiency disease (disorder)	Inferred relationship	Some
Hereditary factor VIII deficiency disease without inhibitor (disorder)	est un(e) (attribut)	True	Hereditary factor VIII deficiency disease (disorder)	Inferred relationship	Some
Carrier of hereditary factor VIII deficiency disease (finding)	est un(e) (attribut)	False	Hereditary factor VIII deficiency disease (disorder)	Inferred relationship	Some
Hereditary factor VIII deficiency disease with inhibitor (disorder)	est un(e) (attribut)	True	Hereditary factor VIII deficiency disease (disorder)	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
100331000172111	hémophilie A	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
1225870016	Congenital factor VIII deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2787090010	Hereditary factor VIII deficiency disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
412821000241112	carence héréditaire en facteur VIII (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
47356012	Hemophilia A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
47359017	Hereditary factor VIII deficiency disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
47360010	Classical hemophilia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
47361014	AHG deficiency disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
47362019	Sex-linked factor VIII deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
47363012	Congenital factor VIII deficiency disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
483814018	Haemophilia A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
483815017	Classical haemophilia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
576561000172110	carence héréditaire en facteur VIII	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)