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254216006: Hereditary erythrokeratolysis (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Abnormal keratinization\Disorder of keratinisation\Inherited disorder of keratinisation\Hereditary erythrokeratolysis

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Hereditary erythrokeratolysis
\Integumentary system finding\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Hereditary erythrokeratolysis
\Integumentary system finding\Abnormal keratinization\Disorder of keratinisation\Inherited disorder of keratinisation\Hereditary erythrokeratolysis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Hereditary erythrokeratolysis
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Hereditary erythrokeratolysis
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Hereditary erythrokeratolysis
\Disease\Disorder of body system\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Hereditary erythrokeratolysis

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
Hereditary erythrokeratolysis	Is a	Inherited disorder of keratinisation	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary erythrokeratolysis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary erythrokeratolysis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary erythrokeratolysis	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary erythrokeratolysis	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary erythrokeratolysis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary erythrokeratolysis	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary erythrokeratolysis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary erythrokeratolysis	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary erythrokeratolysis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary erythrokeratolysis	Finding site	Integumentary system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary erythrokeratolysis	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary erythrokeratolysis	Interprets	Keratinisation	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary erythrokeratolysis	Finding site	Integumentary system structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary erythrokeratolysis	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Keratolytic winter erythema	Is a	True	Hereditary erythrokeratolysis	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratolysis exfoliativa (disorder)	Is a	True	Hereditary erythrokeratolysis	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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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
378442016	Hereditary erythrokeratolysis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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
5082821000241115	érythrokératolyse héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5082821000241115	érythrokératolyse héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module