16922007: Hereditary coagulation factor deficiency (disorder)

SNOMED CT Concept\constatation clinique\...

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

\Disease\Genetic disease\maladie héréditaire\Hereditary coagulation factor deficiency
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

28648014 Hereditary coagulation factor deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

345131000077110 déficit héréditaire en facteur de coagulation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

50013381000188111 déficit héréditaire en facteurs de coagulation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

629941000077111 déficit héréditaire en facteur de coagulation (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

744042017 Hereditary coagulation factor deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary coagulation factor deficiency	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Hereditary coagulation factor deficiency	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Hereditary coagulation factor deficiency	est un(e) (attribut)	Coagulation factor deficiency syndrome	true	Inferred relationship	Some
Hereditary coagulation factor deficiency	est un(e) (attribut)	Hereditary disorder of hematologic system	false	Inferred relationship	Some
Hereditary coagulation factor deficiency	est un(e) (attribut)	Hereditary disorder by system	false	Inferred relationship	Some
Hereditary coagulation factor deficiency	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Hereditary coagulation factor deficiency	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Hereditary coagulation factor deficiency	est un(e) (attribut)	maladie héréditaire	true	Inferred relationship	Some
Hereditary coagulation factor deficiency	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary combined coagulation factor deficiency (disorder)	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Factor XIII deficiency disease	est un(e) (attribut)	False	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor VIII deficiency disease (disorder)	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor I deficiency disease	est un(e) (attribut)	False	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor II deficiency disease	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor X deficiency disease	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor VII deficiency disease (disorder)	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor XII deficiency disease	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor XI deficiency disease (disorder)	est un(e) (attribut)	False	Hereditary coagulation factor deficiency	Inferred relationship	Some
Familial multiple factor deficiency syndrome	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor V deficiency disease	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor XIII deficiency disease (disorder)	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor I deficiency disease	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Hereditary factor IX deficiency disease (disorder)	est un(e) (attribut)	False	Hereditary coagulation factor deficiency	Inferred relationship	Some
Congenital plasminogen activator inhibitor deficiency type 1 (disorder)	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome	est un(e) (attribut)	True	Hereditary coagulation factor deficiency	Inferred relationship	Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)