254215005: Erythrokeratoderma (disorder)

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

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

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

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

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

378441011 Erythrokeratoderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

645076019 Erythrokeratoderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

966401000172112 erythrokératodermie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Erythrokeratoderma	Is a	Inherited disorder of keratinisation	true	Inferred relationship	Some
Erythrokeratoderma	Finding site	Skin structure	false	Inferred relationship	Some	1
Erythrokeratoderma	Occurrence	Congenital	false	Inferred relationship	Some
Erythrokeratoderma	Associated morphology	anomalie congénitale	false	Inferred relationship	Some	1
Erythrokeratoderma	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Some
Erythrokeratoderma	Associated morphology	anomalie congénitale	false	Inferred relationship	Some	1
Erythrokeratoderma	Finding site	Skin structure	false	Inferred relationship	Some	1
Erythrokeratoderma	Occurrence	Congenital	false	Inferred relationship	Some	2
Erythrokeratoderma	Associated morphology	anomalie du développement	false	Inferred relationship	Some	2
Erythrokeratoderma	Finding site	Skin structure	false	Inferred relationship	Some	2
Erythrokeratoderma	Finding site	Structure of integumentary system (body structure)	false	Inferred relationship	Some
Erythrokeratoderma	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Erythrokeratoderma	Interprets	Keratinization	true	Inferred relationship	Some	1
Erythrokeratoderma	Finding site	Structure of integumentary system (body structure)	true	Inferred relationship	Some	2
Erythrokeratoderma	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	2

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

Reference Sets