84048006: Familial multiple factor deficiency syndrome, type I (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 I

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

\Disease\Genetic disease\maladie héréditaire\Hereditary coagulation factor deficiency\Familial multiple factor deficiency syndrome\Familial multiple factor deficiency syndrome, type I
\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 I
\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 I

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

139364010 Familial multiple factor deficiency syndrome, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
139365011 FMFD syndrome, type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
139366012 Factor V and factor VIII deficiency en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
139367015 Factor V AND factor VIII deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
825809015 Familial multiple factor deficiency syndrome, type I (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 I	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type I	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type I	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type I	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type I	est un(e) (attribut)	Familial multiple factor deficiency syndrome	true	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type I	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