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254215005: Erythrokeratoderma (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation fonctionnelle\Abnormal keratinisation\Disorder of keratinisation\Inherited disorder of keratinization\Erythrokeratoderma

\Integumentary system finding\troubles tégumentaires\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma
\Integumentary system finding\troubles tégumentaires\Disorder of keratinisation\Inherited disorder of keratinization\Erythrokeratoderma
\Integumentary system finding\Abnormal keratinisation\Disorder of keratinisation\Inherited disorder of keratinization\Erythrokeratoderma

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma
\Disease\affection d'un système corporel\troubles tégumentaires\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma
\Disease\affection d'un système corporel\troubles tégumentaires\Disorder of keratinisation\Inherited disorder of keratinization\Erythrokeratoderma

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
Erythrokeratoderma	localisation d'une constatation (attribut)	Structure of integumentary system (body structure)	true	Inferred relationship	Some	2
Erythrokeratoderma	morphologie associée (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some	2
Erythrokeratoderma	morphologie associée (attribut)	Congenital anomaly	false	Inferred relationship	Some	1
Erythrokeratoderma	est défini par la manifestation de (attribut)	Abnormal keratinisation	false	Inferred relationship	Some
Erythrokeratoderma	morphologie associée (attribut)	Congenital anomaly	false	Inferred relationship	Some	1
Erythrokeratoderma	localisation d'une constatation (attribut)	structure de la peau	false	Inferred relationship	Some	1
Erythrokeratoderma	survenue (attribut)	congénital	false	Inferred relationship	Some	2
Erythrokeratoderma	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	2
Erythrokeratoderma	localisation d'une constatation (attribut)	structure de la peau	false	Inferred relationship	Some	2
Erythrokeratoderma	localisation d'une constatation (attribut)	structure de la peau	false	Inferred relationship	Some	1
Erythrokeratoderma	survenue (attribut)	congénital	false	Inferred relationship	Some
Erythrokeratoderma	est un(e) (attribut)	Inherited disorder of keratinization	true	Inferred relationship	Some
Erythrokeratoderma	localisation d'une constatation (attribut)	Structure of integumentary system (body structure)	false	Inferred relationship	Some
Erythrokeratoderma	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Erythrokeratoderma	interprète (attribut)	Keratinization, function (observable entity)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hypotrichosis and deafness syndrome	est un(e) (attribut)	True	Erythrokeratoderma	Inferred relationship	Some
Mutilating keratoderma	est un(e) (attribut)	True	Erythrokeratoderma	Inferred relationship	Some
Erythrokeratodermia cardiomyopathy syndrome	est un(e) (attribut)	True	Erythrokeratoderma	Inferred relationship	Some
Erythrokeratoderma en cocardes (disorder)	est un(e) (attribut)	True	Erythrokeratoderma	Inferred relationship	Some
Congenital keratoderma	est un(e) (attribut)	True	Erythrokeratoderma	Inferred relationship	Some
Erythrokeratodermia variabilis	est un(e) (attribut)	False	Erythrokeratoderma	Inferred relationship	Some
Ichthyosiform erythroderma	est un(e) (attribut)	True	Erythrokeratoderma	Inferred relationship	Some
Erythrokeratoderma progressiva of Gottron	est un(e) (attribut)	True	Erythrokeratoderma	Inferred relationship	Some
Spinocerebellar ataxia type 34 (disorder)	est un(e) (attribut)	True	Erythrokeratoderma	Inferred relationship	Some
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder)	est un(e) (attribut)	False	Erythrokeratoderma	Inferred relationship	Some

Reference Sets

Canada English language reference set (foundation metadata concept)

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

Description inactivation indicator reference set

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
378441011	Erythrokeratoderma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
561401000241119	erythrokératodermie (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
645076019	Erythrokeratoderma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
966401000172112	erythrokératodermie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)