6874009: Congenital keratoderma (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin finding\...

\Rough skin (finding)\Congenital keratoderma

\Disorder of skin (disorder)\Keratoderma (disorder)\Congenital keratoderma

\General finding of soft tissue\Skin finding\Rough skin (finding)\Congenital keratoderma
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Keratoderma (disorder)\Congenital keratoderma
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Keratoderma (disorder)\Congenital keratoderma

\Functional finding\Abnormal keratinization\...

\Rough skin (finding)\Congenital keratoderma

\Disorder of keratinisation\Inherited disorder of keratinisation\Erythrokeratoderma\Congenital keratoderma

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Erythrokeratoderma\Congenital keratoderma
\Integumentary system finding\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Erythrokeratoderma\Congenital keratoderma
\Integumentary system finding\Disorder of integument\Disorder involving the integument of fetus OR newborn\Congenital keratoderma
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Keratoderma (disorder)\Congenital keratoderma
\Integumentary system finding\Skin finding\Rough skin (finding)\Congenital keratoderma
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Keratoderma (disorder)\Congenital keratoderma
\Integumentary system finding\Abnormal keratinization\Rough skin (finding)\Congenital keratoderma
\Integumentary system finding\Abnormal keratinization\Disorder of keratinisation\Inherited disorder of keratinisation\Erythrokeratoderma\Congenital keratoderma

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Erythrokeratoderma\Congenital keratoderma
\Disease\Disorder of foetus and/or newborn\Disorder involving the integument of fetus OR newborn\Congenital keratoderma
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital keratoderma
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Erythrokeratoderma\Congenital keratoderma
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Erythrokeratoderma\Congenital keratoderma
\Disease\Disorder of body system\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Erythrokeratoderma\Congenital keratoderma
\Disease\Disorder of body system\Disorder of integument\Disorder involving the integument of fetus OR newborn\Congenital keratoderma
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Keratoderma (disorder)\Congenital keratoderma
\Disease\Keratosis (disorder)\Keratoderma (disorder)\Congenital keratoderma
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Keratoderma (disorder)\Congenital keratoderma

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital keratoderma	Is a	Erythrokeratoderma	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital keratoderma	Is a	Skin lesion	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital keratoderma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital keratoderma	Associated morphology	Hyperkeratosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital keratoderma	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital keratoderma	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital keratoderma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital keratoderma	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital keratoderma	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital keratoderma	Associated morphology	Hyperkeratosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital keratoderma	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Congenital keratoderma	Is a	Keratoderma (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital keratoderma	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital keratoderma	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital keratoderma	Interprets	Keratinisation	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital keratoderma	Is a	Keratosis (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital keratoderma	Is a	Rough skin (finding)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital keratoderma	Is a	Disorder involving the integument of fetus OR newborn	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A hereditary palmoplantar keratoderma with characteristics of the combination of bilateral mutilating transgredient palmoplantar keratoderma and periorificial keratotic plaques.	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Mutilating keratoderma	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratosis palmaris et plantaris	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Diffuse palmoplantar keratoderma	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratoderma areata	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratoderma with pachyonychia congenita	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder)	Is a	True	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratoderma with mental retardation and spastic paraplegia	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratoderma punctata	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome (disorder)	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Erythrokeratodermia variabilis (disorder)	Is a	True	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
MEDNIK syndrome	Is a	True	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratoderma hereditarium mutilans with ichthyosis syndrome	Is a	True	Congenital keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
12370013	Congenital keratoderma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
808609014	Congenital keratoderma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
12370013	Congenital keratoderma	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
12370013	Congenital keratoderma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
808609014	Congenital keratoderma (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
808609014	Congenital keratoderma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4411311000241112	kératodermie congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4411311000241112	kératodermie congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module