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254215005: Erythrokeratoderma (disorder)

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
378441011 Erythrokeratoderma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
3439951001000111 Erythrokeratodermie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
966401000172112 erythrokératodermie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
966401000172112 erythrokératodermie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3439951001000111 Erythrokeratodermie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

15 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythrokeratoderma Is a Inherited disorder of keratinisation true Inferred relationship Existential restriction modifier (core metadata concept)
Erythrokeratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Erythrokeratoderma Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Erythrokeratoderma Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Erythrokeratoderma Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier (core metadata concept)
Erythrokeratoderma Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Erythrokeratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Erythrokeratoderma Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Erythrokeratoderma Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Erythrokeratoderma Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Erythrokeratoderma Finding site Integumentary system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Erythrokeratoderma Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Erythrokeratoderma Interprets Keratinisation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Erythrokeratoderma Finding site Integumentary system structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Erythrokeratoderma Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Erythrokeratoderma progressiva of Gottron Is a True Erythrokeratoderma Inferred relationship Existential restriction modifier (core metadata concept)
Congenital keratoderma Is a True Erythrokeratoderma Inferred relationship Existential restriction modifier (core metadata concept)
Erythrokeratodermia variabilis (disorder) Is a False Erythrokeratoderma Inferred relationship Existential restriction modifier (core metadata concept)
Erythrokeratoderma en cocardes (disorder) Is a True Erythrokeratoderma Inferred relationship Existential restriction modifier (core metadata concept)
Ichthyosiform erythroderma Is a True Erythrokeratoderma Inferred relationship Existential restriction modifier (core metadata concept)
An autosomal dominant cerebellar ataxia type I that is characterized by papulosquamous, ichthyosiform plaques on the limbs appearing shortly after birth and later manifestations including progressive ataxia, dysarthria, nystagmus and decreased reflexes. Is a True Erythrokeratoderma Inferred relationship Existential restriction modifier (core metadata concept)
MEDNIK syndrome Is a False Erythrokeratoderma Inferred relationship Existential restriction modifier (core metadata concept)
Hypotrichosis and deafness syndrome (disorder) Is a True Erythrokeratoderma Inferred relationship Existential restriction modifier (core metadata concept)
Mutilating keratoderma Is a True Erythrokeratoderma Inferred relationship Existential restriction modifier (core metadata concept)
Erythrokeratodermia cardiomyopathy syndrome Is a True Erythrokeratoderma Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

GB English

US English

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