6874009: congenitale keratoderma (aandoening)

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

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

\Rough skin (finding)\Congenital keratoderma

\Disorder of skin (disorder)\Hyperplasia of skin (disorder)\Keratoderma\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)\Hyperplasia of skin (disorder)\Keratoderma\Congenital keratoderma
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Hyperplasia of skin (disorder)\Keratoderma\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\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)\Hyperplasia of skin (disorder)\Keratoderma\Congenital keratoderma
\Integumentary system finding\Skin finding\Rough skin (finding)\Congenital keratoderma
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Hyperplasia of skin (disorder)\Keratoderma\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\Hereditary disorder of the integument\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 (disorder)\Congenital keratoderma
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinisation\Erythrokeratoderma\Congenital keratoderma
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\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)\Hyperplasia of skin (disorder)\Keratoderma\Congenital keratoderma
\Disease\Keratosis\Keratoderma\Congenital keratoderma
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Hyperplasia of skin (disorder)\Keratoderma\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	Some
Congenital keratoderma	Is a	Skin lesion	false	Inferred relationship	Some
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	1
Congenital keratoderma	Occurrence	Congenital	false	Inferred relationship	Some
Congenital keratoderma	Associated morphology	Hyperkeratosis	false	Inferred relationship	Some	1
Congenital keratoderma	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Some
Congenital keratoderma	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	2
Congenital keratoderma	Occurrence	Congenital	false	Inferred relationship	Some	3
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Some	3
Congenital keratoderma	Associated morphology	gebrekkige ontwikkeling (afwijkende morfologie)	false	Inferred relationship	Some	3
Congenital keratoderma	Occurrence	Congenital	true	Inferred relationship	Some	4
Congenital keratoderma	Associated morphology	Hyperkeratosis	true	Inferred relationship	Some	4
Congenital keratoderma	Finding site	Skin structure	true	Inferred relationship	Some	4
Congenital keratoderma	Is a	Keratoderma	true	Inferred relationship	Some
Congenital keratoderma	Is a	Congenital disease (disorder)	true	Inferred relationship	Some
Congenital keratoderma	Has interpretation	Abnormal	true	Inferred relationship	Some	2
Congenital keratoderma	Interprets	Keratinization	true	Inferred relationship	Some	2
Congenital keratoderma	Is a	Keratosis	false	Inferred relationship	Some
Congenital keratoderma	Is a	Rough skin (finding)	true	Inferred relationship	Some
Congenital keratoderma	Is a	Disorder involving the integument of fetus OR newborn	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital palmoplantar and perioral keratoderma of Olmsted	Is a	False	Congenital keratoderma	Inferred relationship	Some
Mutilating keratoderma	Is a	False	Congenital keratoderma	Inferred relationship	Some
Keratosis palmaris et plantaris	Is a	False	Congenital keratoderma	Inferred relationship	Some
Diffuse palmoplantar keratoderma	Is a	False	Congenital keratoderma	Inferred relationship	Some
keratoderma areata	Is a	False	Congenital keratoderma	Inferred relationship	Some
keratoderma met pachyonychia congenita (aandoening)	Is a	False	Congenital keratoderma	Inferred relationship	Some
Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder)	Is a	True	Congenital keratoderma	Inferred relationship	Some
Keratoderma with mental retardation and spastic paraplegia	Is a	False	Congenital keratoderma	Inferred relationship	Some
Keratoderma punctata	Is a	False	Congenital keratoderma	Inferred relationship	Some
Naxos disease	Is a	False	Congenital keratoderma	Inferred relationship	Some
Erythrokeratodermia variabilis	Is a	True	Congenital keratoderma	Inferred relationship	Some
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder)	Is a	True	Congenital keratoderma	Inferred relationship	Some
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder)	Is a	True	Congenital keratoderma	Inferred relationship	Some

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
10535181000146118	congenitale keratoderma	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
10535191000146116	congenitale keratoderma (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
10535201000146119	aangeboren keratoderma	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
11558261000146116	keratoderma congenitalis	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)