703504006: Congenital reticular ichthyosiform erythroderma (disorder)

SNOMED CT Concept\Clinical finding\...

\Functional finding\Abnormal keratinization\Disorder of keratinization\Inherited disorder of keratinization\Erythrokeratoderma\Ichthyosiform erythroderma\Congenital ichthyosiform erythroderma\Congenital reticular ichthyosiform erythroderma

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma\Ichthyosiform erythroderma\Congenital ichthyosiform erythroderma\Congenital reticular ichthyosiform erythroderma
\Integumentary system finding\Disorder of integument\Disorder of keratinization\Inherited disorder of keratinization\Erythrokeratoderma\Ichthyosiform erythroderma\Congenital ichthyosiform erythroderma\Congenital reticular ichthyosiform erythroderma
\Integumentary system finding\Abnormal keratinization\Disorder of keratinization\Inherited disorder of keratinization\Erythrokeratoderma\Ichthyosiform erythroderma\Congenital ichthyosiform erythroderma\Congenital reticular ichthyosiform erythroderma

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma\Ichthyosiform erythroderma\Congenital ichthyosiform erythroderma\Congenital reticular ichthyosiform erythroderma
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Congenital reticular ichthyosiform erythroderma
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma\Ichthyosiform erythroderma\Congenital ichthyosiform erythroderma\Congenital reticular ichthyosiform erythroderma
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma\Ichthyosiform erythroderma\Congenital ichthyosiform erythroderma\Congenital reticular ichthyosiform erythroderma
\Disease\Disorder of body system\Disorder of integument\Disorder of keratinization\Inherited disorder of keratinization\Erythrokeratoderma\Ichthyosiform erythroderma\Congenital ichthyosiform erythroderma\Congenital reticular ichthyosiform erythroderma
\Disease\Congenital disease\Congenital ichthyosiform erythroderma\Congenital reticular ichthyosiform erythroderma

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3008765012 Congenital reticular ichthyosiform erythroderma (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3008789017 Congenital reticular ichthyosiform erythroderma en Synonym Active Entire term case insensitive SNOMED CT core module

3008812013 Ichthyosis with confetti en Synonym Active Entire term case insensitive SNOMED CT core module

3008838013 Ichthyosis variegata en Synonym Active Entire term case insensitive SNOMED CT core module

3008848010 CRIE - Congenital reticular ichthyosiform erythroderma en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital reticular ichthyosiform erythroderma	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Congenital reticular ichthyosiform erythroderma	Is a	Congenital ichthyosiform erythroderma	true	Inferred relationship	Existential restriction modifier
Congenital reticular ichthyosiform erythroderma	Is a	Hereditary disorder of the integument	false	Inferred relationship	Existential restriction modifier
Congenital reticular ichthyosiform erythroderma	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Existential restriction modifier
Congenital reticular ichthyosiform erythroderma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Congenital reticular ichthyosiform erythroderma	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Congenital reticular ichthyosiform erythroderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Congenital reticular ichthyosiform erythroderma	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Congenital reticular ichthyosiform erythroderma	Finding site	Structure of integumentary system	false	Inferred relationship	Existential restriction modifier
Congenital reticular ichthyosiform erythroderma	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	1
Congenital reticular ichthyosiform erythroderma	Interprets	Keratinization, function	true	Inferred relationship	Existential restriction modifier	1
Congenital reticular ichthyosiform erythroderma	Finding site	Structure of integumentary system	true	Inferred relationship	Existential restriction modifier	2
Congenital reticular ichthyosiform erythroderma	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3008765012	Congenital reticular ichthyosiform erythroderma (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3008789017	Congenital reticular ichthyosiform erythroderma	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3008812013	Ichthyosis with confetti	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3008838013	Ichthyosis variegata	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3008848010	CRIE - Congenital reticular ichthyosiform erythroderma	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module