64315007: Familial multiple factor deficiency syndrome, type III (disorder)

SNOMED CT Concept\constatation clinique\...

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

\Combined coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type III

\Hereditary coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type III

\Disease\Genetic disease\maladie héréditaire\Hereditary coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type III
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Combined coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type III
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type III

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

106910018 Familial multiple factor deficiency syndrome, type III en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

106912014 FMFD syndrome, type III en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

106913016 Factors II, VII, IX AND X deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

803695011 Familial multiple factor deficiency syndrome, type III (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial multiple factor deficiency syndrome, type III	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type III	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type III	est un(e) (attribut)	Familial multiple factor deficiency syndrome	true	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type III	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type III	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type III	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some

Inbound Relationships

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This concept is not in any reference sets