51626007: Werner syndrome (disorder)

SNOMED CT Concept\constatation clinique\...

\Skin AND/OR mucosa finding (finding)\Skin finding\affection de la peau (trouble)\...

\Premature aging syndrome (disorder)\syndrome de Werner (trouble)

\Congenital anomaly of skin\syndrome de Werner (trouble)

\constatation à propos du développement physiologique\anomalie staturale\syndrome de Werner (trouble)

\constatation générale à propos des tissus mous\Skin finding\affection de la peau (trouble)\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\constatation générale à propos des tissus mous\Skin finding\affection de la peau (trouble)\Congenital anomaly of skin\syndrome de Werner (trouble)
\constatation générale à propos des tissus mous\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\constatation générale à propos des tissus mous\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Congenital anomaly of skin\syndrome de Werner (trouble)

\constatation générale à propos de l'observation du patient\Body measurement finding\Height / growth finding\General finding of height\anomalie staturale\syndrome de Werner (trouble)

\Integumentary system finding\troubles tégumentaires\Hereditary disorder of the integument\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Integumentary system finding\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Integumentary system finding\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Congenital anomaly of skin\syndrome de Werner (trouble)
\Integumentary system finding\troubles tégumentaires\Congenital anomaly of integument\Congenital anomaly of skin\syndrome de Werner (trouble)
\Integumentary system finding\Skin finding\affection de la peau (trouble)\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Integumentary system finding\Skin finding\affection de la peau (trouble)\Congenital anomaly of skin\syndrome de Werner (trouble)

\Disease\Genetic disease\maladie héréditaire\syndrome familial avec prédisposition aux cancers (trouble)\syndrome de Werner (trouble)
\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\syndrome de Werner (trouble)
\Disease\Genetic disease\maladie héréditaire\Inborn error of metabolism\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\syndrome de Werner (trouble)
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Disease\affection d'un système corporel\troubles tégumentaires\Hereditary disorder of the integument\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Disease\affection d'un système corporel\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Disease\affection d'un système corporel\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Congenital anomaly of skin\syndrome de Werner (trouble)
\Disease\affection d'un système corporel\troubles tégumentaires\Congenital anomaly of integument\Congenital anomaly of skin\syndrome de Werner (trouble)
\Disease\trouble métabolique\Inborn error of metabolism\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome (disorder)\syndrome de malformations multisystémiques\Multiple malformation syndrome with senile-like appearance\syndrome de Werner (trouble)
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\syndrome de Werner (trouble)
\Disease\Congenital disease\Inborn error of metabolism\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Disease\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Premature aging syndrome (disorder)\syndrome de Werner (trouble)
\Disease\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Congenital anomaly of skin\syndrome de Werner (trouble)
\Disease\trouble du développement\Developmental hereditary disorder\syndrome de Werner (trouble)
\Disease\trouble du développement\Congenital malformation\Congenital malformation syndrome (disorder)\syndrome de malformations multisystémiques\Multiple malformation syndrome with senile-like appearance\syndrome de Werner (trouble)
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\syndrome de Werner (trouble)
\Disease\trouble du développement\anomalie staturale\syndrome de Werner (trouble)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
syndrome de Werner (trouble)	morphologie associée (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some	1
syndrome de Werner (trouble)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
syndrome de Werner (trouble)	localisation d'une constatation (attribut)	structure de la peau	true	Inferred relationship	Some	1
syndrome de Werner (trouble)	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
syndrome de Werner (trouble)	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
syndrome de Werner (trouble)	interprète (attribut)	Height / growth measure	true	Inferred relationship	Some	2
syndrome de Werner (trouble)	est un(e) (attribut)	Congenital anomaly of skin	true	Inferred relationship	Some
syndrome de Werner (trouble)	est un(e) (attribut)	Premature aging syndrome (disorder)	true	Inferred relationship	Some
syndrome de Werner (trouble)	morphologie associée (attribut)	Congenital malformation	false	Inferred relationship	Some
syndrome de Werner (trouble)	est un(e) (attribut)	Progeria syndrome	false	Inferred relationship	Some
syndrome de Werner (trouble)	est un(e) (attribut)	Multiple malformation syndrome with senile-like appearance	true	Inferred relationship	Some
syndrome de Werner (trouble)	est un(e) (attribut)	anomalie staturale	true	Inferred relationship	Some
syndrome de Werner (trouble)	est un(e) (attribut)	syndrome familial avec prédisposition aux cancers (trouble)	true	Inferred relationship	Some
syndrome de Werner (trouble)	survenue (attribut)	congénital	true	Inferred relationship	Some	1
syndrome de Werner (trouble)	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	1
syndrome de Werner (trouble)	localisation d'une constatation (attribut)	structure de la peau	false	Inferred relationship	Some	2
syndrome de Werner (trouble)	survenue (attribut)	congénital	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

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

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Id	Description	Lang	Type	Status	Case?	Module
1231007018	Pangeria	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1231008011	Adult progeria	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1783826013	Adult premature ageing syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1784214017	Adult premature aging syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
438071000241114	syndrome de Werner (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
789546011	Werner syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
85980017	Werner syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
85981018	Progeria of the adult	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
911521000172110	syndrome de Werner	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
930831000172113	progéria de l'adulte	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)