FHIR © HL7.org | Server Home | FHIR Server FHIR Server 4.0.1 | FHIR Version n/a User: [n/a]

88518009: Wilson's disease (disorder)

SNOMED CT Concept\constatation clinique\...

\Viscus structure finding (finding)\constatation à propos d'un organe abdominal\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Wilson's disease

\Digestive system finding (finding)\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Wilson's disease
\Digestive system finding (finding)\maladie de l'appareil digestif\Digestive system hereditary disorder\Wilson's disease
\Digestive system finding (finding)\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\troubles métaboliques et génétiques affectant le foie\Wilson's disease

\constatation à propos d'une région de la tête et du cou\Head finding (finding)\...

\constatation à propos l'encéphale\Disorder of brain (disorder)\Degenerative brain disorder\Wilson's disease

\affection de la tête\Disorder of brain (disorder)\Degenerative brain disorder\Wilson's disease

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease
\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Digestive system hereditary disorder\Wilson's disease
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Wilson's disease
\Disease\affection dégénérative\maladie dégénérative du système nerveux central\Hereditary degenerative disease of central nervous system\Wilson's disease
\Disease\affection dégénérative\maladie dégénérative du système nerveux central\Degenerative brain disorder\Wilson's disease
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease
\Disease\affection d'un système corporel\Hereditary disorder by system\Digestive system hereditary disorder\Wilson's disease
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Wilson's disease
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\System disorder of the nervous system (disorder)\Disorder presenting primarily with chorea (disorder)\Wilson's disease
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Degenerative brain disorder\Wilson's disease
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Hereditary degenerative disease of central nervous system\Wilson's disease
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Degenerative brain disorder\Wilson's disease
\Disease\affection d'un système corporel\maladie de l'appareil digestif\Digestive system hereditary disorder\Wilson's disease
\Disease\affection d'un système corporel\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\troubles métaboliques et génétiques affectant le foie\Wilson's disease
\Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Wilson's disease
\Disease\affection de la tête\Disorder of brain (disorder)\Degenerative brain disorder\Wilson's disease
\Disease\trouble métabolique\troubles métaboliques et génétiques affectant le foie\Wilson's disease
\Disease\trouble métabolique\troubles du métabolisme des minéraux (trouble)\Disorder of copper metabolism\Wilson's disease

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
Wilson's disease	localisation d'une constatation (attribut)	structure du tissu encéphalique	true	Inferred relationship	Some	2
Wilson's disease	morphologie associée (attribut)	Degenerative abnormality	true	Inferred relationship	Some	2
Wilson's disease	morphologie associée (attribut)	Degenerative abnormality	true	Inferred relationship	Some	1
Wilson's disease	morphologie associée (attribut)	Degenerative abnormality	true	Inferred relationship	Some	3
Wilson's disease	localisation d'une constatation (attribut)	Body tissue structure	true	Inferred relationship	Some	3
Wilson's disease	est un(e) (attribut)	Hereditary degenerative disease of central nervous system	true	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	maladie dégénérative du système nerveux central	false	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	Disorder of brain (disorder)	false	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	lésion cérébrale	false	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	Lesion of liver	false	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	Degenerative brain disorder	true	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	Disorder presenting primarily with chorea (disorder)	true	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	Hereditary disorder of nervous system	false	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	troubles métaboliques et génétiques affectant le foie	true	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	Disorder of copper metabolism	true	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	Digestive system hereditary disorder	true	Inferred relationship	Some
Wilson's disease	est un(e) (attribut)	affection dégénérative	false	Inferred relationship	Some
Wilson's disease	localisation d'une constatation (attribut)	foie	true	Inferred relationship	Some	1
Wilson's disease	localisation d'une constatation (attribut)	structure du tissu encéphalique	false	Inferred relationship	Some	1
Wilson's disease	morphologie associée (attribut)	dégénérescence	false	Inferred relationship	Some	1
Wilson's disease	morphologie associée (attribut)	dégénérescence	false	Inferred relationship	Some	2
Wilson's disease	localisation d'une constatation (attribut)	foie	false	Inferred relationship	Some	2
Wilson's disease	morphologie associée (attribut)	dégénérescence	false	Inferred relationship	Some	3
Wilson's disease	morphologie associée (attribut)	dégénérescence	false	Inferred relationship	Some	4
Wilson's disease	localisation d'une constatation (attribut)	structure du tissu encéphalique	false	Inferred relationship	Some	3
Wilson's disease	localisation d'une constatation (attribut)	Body tissue structure	false	Inferred relationship	Some	4
Wilson's disease	morphologie associée (attribut)	dégénérescence	false	Inferred relationship	Some	1
Wilson's disease	localisation d'une constatation (attribut)	foie	false	Inferred relationship	Some	1
Wilson's disease	localisation d'une constatation (attribut)	structure du tissu encéphalique	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Westphal-Strumpell syndrome	est un(e) (attribut)	True	Wilson's disease	Inferred relationship	Some
Hypoparathyroidism due to Wilson disease	Due to	True	Wilson's disease	Inferred relationship	Some	3
Chorea co-occurrent and due to Wilson disease (disorder)	Due to	True	Wilson's disease	Inferred relationship	Some	3
Chorea co-occurrent and due to Wilson disease (disorder)	est un(e) (attribut)	True	Wilson's disease	Inferred relationship	Some

Reference Sets

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

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
146760018	Wilson's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
146761019	Hepatolenticular degeneration syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
146762014	Copper storage disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
146763016	Cerebral pseudosclerosis	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
146764010	Westphal-Strümpell syndrome	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
146765011	Westphal-Strumpell syndrome	en	Synonym (core metadata concept)	Inactive	Entire term case sensitive (core metadata concept)	SNOMED CT core
193521000172110	maladie de Wilson	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
2840410019	Wilson disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3393319011	Maladie de Wilson	fr	Synonym (core metadata concept)	Inactive	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
479641000241119	maladie de Wilson (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
508067014	Hepatocerebral degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508068016	Hepatolenticular degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508069012	Kinnier-Wilson disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
508070013	Neurohepatic degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508071012	Progressive lenticular degeneration	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
508072017	WD - Wilson's disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
831218010	Wilson's disease (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core