61551003: Familial multiple factor deficiency syndrome, type VI (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 VI

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

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

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

102251013 Familial multiple factor deficiency syndrome, type VI en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
102252018 FMFD syndrome, type VI en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
102253011 Factor IX and factor XI deficiency en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
102254017 Factor IX AND factor XI deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
800626019 Familial multiple factor deficiency syndrome, type VI (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 VI	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type VI	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type VI	est un(e) (attribut)	Familial multiple factor deficiency syndrome	true	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type VI	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type VI	est défini par la manifestation de (attribut)	constatation sur le système hémostatique	false	Inferred relationship	Some
Familial multiple factor deficiency syndrome, type VI	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