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254216006: Hereditary erythrokeratolysis (disorder)

SNOMED CT Concept\Clinical finding\...

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

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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinization\Hereditary erythrokeratolysis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinization\Hereditary erythrokeratolysis
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Inherited disorder of keratinization\Hereditary erythrokeratolysis
\Disease\Disorder of body system\Disorder of integument\Disorder of keratinization\Inherited disorder of keratinization\Hereditary erythrokeratolysis

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

378442016 Hereditary erythrokeratolysis en Synonym Active Entire term case insensitive SNOMED CT core module

645077011 Hereditary erythrokeratolysis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary erythrokeratolysis	Is a	Inherited disorder of keratinization	true	Inferred relationship	Existential restriction modifier
Hereditary erythrokeratolysis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Hereditary erythrokeratolysis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Hereditary erythrokeratolysis	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Existential restriction modifier
Hereditary erythrokeratolysis	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Hereditary erythrokeratolysis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Hereditary erythrokeratolysis	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Hereditary erythrokeratolysis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Hereditary erythrokeratolysis	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Hereditary erythrokeratolysis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Hereditary erythrokeratolysis	Finding site	Structure of integumentary system	false	Inferred relationship	Existential restriction modifier
Hereditary erythrokeratolysis	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	1
Hereditary erythrokeratolysis	Interprets	Keratinization, function	true	Inferred relationship	Existential restriction modifier	1
Hereditary erythrokeratolysis	Finding site	Structure of integumentary system	true	Inferred relationship	Existential restriction modifier	2
Hereditary erythrokeratolysis	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Keratolytic winter erythema	Is a	True	Hereditary erythrokeratolysis	Inferred relationship	Existential restriction modifier
Keratolysis exfoliativa	Is a	True	Hereditary erythrokeratolysis	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
378442016	Hereditary erythrokeratolysis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
645077011	Hereditary erythrokeratolysis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module