65768009: Familial multiple factor deficiency syndrome, type II (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 II

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

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

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

109258018 Familial multiple factor deficiency syndrome, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

109259014 FMFD syndrome, type II en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

109261017 Factor VIII AND factor IX deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

805307018 Familial multiple factor deficiency syndrome, type II (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 II	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type II	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type II	est un(e) (attribut)	Familial multiple factor deficiency syndrome	true	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type II	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type II	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type II	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