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254215005: Erythrokeratoderma (disorder)

SNOMED CT Concept\Clinical finding\...

\Functional finding\Abnormal keratinization\Disorder of keratinization\Inherited disorder of keratinization\Erythrokeratoderma

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

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

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

378441011 Erythrokeratoderma en Synonym Active Entire term case insensitive SNOMED CT core module

645076019 Erythrokeratoderma (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
Erythrokeratoderma	Is a	Inherited disorder of keratinization	true	Inferred relationship	Existential restriction modifier
Erythrokeratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Erythrokeratoderma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Erythrokeratoderma	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Erythrokeratoderma	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Existential restriction modifier
Erythrokeratoderma	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Erythrokeratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Erythrokeratoderma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Erythrokeratoderma	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Erythrokeratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Erythrokeratoderma	Finding site	Structure of integumentary system	false	Inferred relationship	Existential restriction modifier
Erythrokeratoderma	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	1
Erythrokeratoderma	Interprets	Keratinization, function	true	Inferred relationship	Existential restriction modifier	1
Erythrokeratoderma	Finding site	Structure of integumentary system	true	Inferred relationship	Existential restriction modifier	2
Erythrokeratoderma	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Erythrokeratoderma progressiva of Gottron	Is a	True	Erythrokeratoderma	Inferred relationship	Existential restriction modifier
Congenital keratoderma	Is a	True	Erythrokeratoderma	Inferred relationship	Existential restriction modifier
Erythrokeratodermia variabilis	Is a	False	Erythrokeratoderma	Inferred relationship	Existential restriction modifier
Erythrokeratoderma en cocardes	Is a	True	Erythrokeratoderma	Inferred relationship	Existential restriction modifier
Ichthyosiform erythroderma	Is a	True	Erythrokeratoderma	Inferred relationship	Existential restriction modifier
Spinocerebellar ataxia type 34	Is a	True	Erythrokeratoderma	Inferred relationship	Existential restriction modifier
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome	Is a	False	Erythrokeratoderma	Inferred relationship	Existential restriction modifier
Hypotrichosis and deafness syndrome	Is a	True	Erythrokeratoderma	Inferred relationship	Existential restriction modifier
Mutilating keratoderma	Is a	True	Erythrokeratoderma	Inferred relationship	Existential restriction modifier
Erythrokeratodermia cardiomyopathy syndrome	Is a	True	Erythrokeratoderma	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
378441011	Erythrokeratoderma	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
645076019	Erythrokeratoderma (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module