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254216006: Hereditary erythrokeratolysis (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation fonctionnelle\Abnormal keratinisation\Disorder of keratinisation\Inherited disorder of keratinization\Hereditary erythrokeratolysis

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

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

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

378442016 Hereditary erythrokeratolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

645077011 Hereditary erythrokeratolysis (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 erythrokeratolysis	localisation d'une constatation (attribut)	Structure of integumentary system (body structure)	true	Inferred relationship	Some	2
Hereditary erythrokeratolysis	morphologie associée (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some	2
Hereditary erythrokeratolysis	est défini par la manifestation de (attribut)	Abnormal keratinisation	false	Inferred relationship	Some
Hereditary erythrokeratolysis	morphologie associée (attribut)	Congenital anomaly	false	Inferred relationship	Some	1
Hereditary erythrokeratolysis	localisation d'une constatation (attribut)	structure de la peau	false	Inferred relationship	Some	1
Hereditary erythrokeratolysis	morphologie associée (attribut)	Congenital anomaly	false	Inferred relationship	Some	1
Hereditary erythrokeratolysis	survenue (attribut)	congénital	false	Inferred relationship	Some	2
Hereditary erythrokeratolysis	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	2
Hereditary erythrokeratolysis	localisation d'une constatation (attribut)	structure de la peau	false	Inferred relationship	Some	2
Hereditary erythrokeratolysis	survenue (attribut)	congénital	false	Inferred relationship	Some
Hereditary erythrokeratolysis	localisation d'une constatation (attribut)	structure de la peau	false	Inferred relationship	Some	1
Hereditary erythrokeratolysis	est un(e) (attribut)	Inherited disorder of keratinization	true	Inferred relationship	Some
Hereditary erythrokeratolysis	localisation d'une constatation (attribut)	Structure of integumentary system (body structure)	false	Inferred relationship	Some
Hereditary erythrokeratolysis	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Hereditary erythrokeratolysis	interprète (attribut)	Keratinization, function (observable entity)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
erythème kératolytique hivernal	est un(e) (attribut)	True	Hereditary erythrokeratolysis	Inferred relationship	Some
Keratolysis exfoliativa	est un(e) (attribut)	True	Hereditary erythrokeratolysis	Inferred relationship	Some

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
378442016	Hereditary erythrokeratolysis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
645077011	Hereditary erythrokeratolysis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core