238834002: Hereditary sclerosing poikiloderma (disorder)

SNOMED CT Concept\constatation clinique\...

\Skin AND/OR mucosa finding (finding)\Skin finding\affection de la peau (trouble)\Degenerative skin disorder (disorder)\état atrophique de la peau (trouble)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma

\constatation générale à propos des tissus mous\Skin finding\affection de la peau (trouble)\Degenerative skin disorder (disorder)\état atrophique de la peau (trouble)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma
\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)\Degenerative skin disorder (disorder)\état atrophique de la peau (trouble)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma

\Integumentary system finding\troubles tégumentaires\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma
\Integumentary system finding\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Degenerative skin disorder (disorder)\état atrophique de la peau (trouble)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma
\Integumentary system finding\Skin finding\affection de la peau (trouble)\Degenerative skin disorder (disorder)\état atrophique de la peau (trouble)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma
\Disease\affection dégénérative\Degenerative skin disorder (disorder)\état atrophique de la peau (trouble)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma
\Disease\affection d'un système corporel\troubles tégumentaires\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma
\Disease\affection d'un système corporel\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Degenerative skin disorder (disorder)\état atrophique de la peau (trouble)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma
\Disease\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\affection de la peau (trouble)\Degenerative skin disorder (disorder)\état atrophique de la peau (trouble)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma

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

357950017 Weary-Kindler syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

357951018 Hereditary sclerosing poikiloderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

627769014 Hereditary sclerosing poikiloderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary sclerosing poikiloderma	localisation d'une constatation (attribut)	structure de la peau	false	Inferred relationship	Some
Hereditary sclerosing poikiloderma	est un(e) (attribut)	Hereditary disorder of the integument	true	Inferred relationship	Some
Hereditary sclerosing poikiloderma	est un(e) (attribut)	affection de la peau (trouble)	false	Inferred relationship	Some
Hereditary sclerosing poikiloderma	morphologie associée (attribut)	Poikiloderma	true	Inferred relationship	Some	1
Hereditary sclerosing poikiloderma	localisation d'une constatation (attribut)	structure de la peau	true	Inferred relationship	Some	1
Hereditary sclerosing poikiloderma	est un(e) (attribut)	Poikiloderma (disorder)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary sclerosing poikiloderma of Weary (disorder)	est un(e) (attribut)	True	Hereditary sclerosing poikiloderma	Inferred relationship	Some
Hereditary acrokeratotic poikiloderma of Weary	est un(e) (attribut)	True	Hereditary sclerosing poikiloderma	Inferred relationship	Some
Kindler's syndrome	est un(e) (attribut)	True	Hereditary sclerosing poikiloderma	Inferred relationship	Some
Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome (disorder)	est un(e) (attribut)	True	Hereditary sclerosing poikiloderma	Inferred relationship	Some

Reference Sets

Canada French language reference set (foundation metadata concept)

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