6874009: Congenital keratoderma (disorder)

SNOMED CT Concept\Clinical finding\...

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

\Rough skin\Congenital keratoderma

\Disorder of skin\Keratoderma\Congenital keratoderma

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

\Functional finding\Abnormal keratinization\...

\Rough skin\Congenital keratoderma

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

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma\Congenital keratoderma
\Integumentary system finding\Disorder of integument\Disorder of keratinization\Inherited disorder of keratinization\Erythrokeratoderma\Congenital keratoderma
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Keratoderma\Congenital keratoderma
\Integumentary system finding\Skin finding\Rough skin\Congenital keratoderma
\Integumentary system finding\Skin finding\Disorder of skin\Keratoderma\Congenital keratoderma
\Integumentary system finding\Abnormal keratinization\Rough skin\Congenital keratoderma
\Integumentary system finding\Abnormal keratinization\Disorder of keratinization\Inherited disorder of keratinization\Erythrokeratoderma\Congenital keratoderma

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma\Congenital keratoderma
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma\Congenital keratoderma
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Inherited disorder of keratinization\Erythrokeratoderma\Congenital keratoderma
\Disease\Disorder of body system\Disorder of integument\Disorder of keratinization\Inherited disorder of keratinization\Erythrokeratoderma\Congenital keratoderma
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Keratoderma\Congenital keratoderma
\Disease\Keratosis\Keratoderma\Congenital keratoderma
\Disease\Congenital disease\Congenital keratoderma
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Keratoderma\Congenital keratoderma

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

Descriptions:

Id Description Lang Type Status Case? Module

12370013 Congenital keratoderma en Synonym Active Entire term case insensitive SNOMED CT core module

808609014 Congenital keratoderma (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital keratoderma	Is a	Erythrokeratoderma	true	Inferred relationship	Existential restriction modifier
Congenital keratoderma	Is a	Skin lesion	false	Inferred relationship	Existential restriction modifier
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Congenital keratoderma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Congenital keratoderma	Associated morphology	Hyperkeratosis	false	Inferred relationship	Existential restriction modifier	1
Congenital keratoderma	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Existential restriction modifier
Congenital keratoderma	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	2
Congenital keratoderma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Congenital keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Congenital keratoderma	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	3
Congenital keratoderma	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	4
Congenital keratoderma	Associated morphology	Hyperkeratosis	true	Inferred relationship	Existential restriction modifier	4
Congenital keratoderma	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	4
Congenital keratoderma	Is a	Keratoderma	true	Inferred relationship	Existential restriction modifier
Congenital keratoderma	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier
Congenital keratoderma	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	2
Congenital keratoderma	Interprets	Keratinization, function	true	Inferred relationship	Existential restriction modifier	2
Congenital keratoderma	Is a	Keratosis	false	Inferred relationship	Existential restriction modifier
Congenital keratoderma	Is a	Rough skin	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital palmoplantar and perioral keratoderma of Olmsted	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Mutilating keratoderma	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Keratosis palmaris et plantaris	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Diffuse palmoplantar keratoderma	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Keratoderma areata	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Keratoderma with pachyonychia congenita	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Palmoplantar hyperkeratosis sclerodactyly syndrome	Is a	True	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Keratoderma with mental retardation and spastic paraplegia	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Keratoderma punctata	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome	Is a	False	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Erythrokeratodermia variabilis	Is a	True	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome	Is a	True	Congenital keratoderma	Inferred relationship	Existential restriction modifier
Keratoderma hereditarium mutilans with ichthyosis syndrome	Is a	True	Congenital keratoderma	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
12370013	Congenital keratoderma	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
808609014	Congenital keratoderma (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module