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24559001: Mutilating keratoderma (disorder)

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

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

\Rough skin (finding)\Rough skin of hands (finding)\Mutilating keratoderma

\Disorder of skin (disorder)\Keratoderma (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disorder of skin (disorder)\Disorder of skin of lower limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disorder of skin (disorder)\Disorder of skin of upper limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma

\Ear and auditory finding\Disorder of auditory system\Auditory system hereditary disorder\Mutilating keratoderma
\Ear and auditory finding\Disorder of auditory system\Hearing disorder (disorder)\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Mutilating keratoderma
\Ear and auditory finding\Disorder of auditory system\Hearing disorder (disorder)\Hearing loss\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Mutilating keratoderma
\Ear and auditory finding\Hearing finding\Hearing disorder (disorder)\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Mutilating keratoderma
\Ear and auditory finding\Hearing finding\Hearing disorder (disorder)\Hearing loss\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Mutilating keratoderma

\Functional finding\Hearing finding\Hearing disorder (disorder)\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Mutilating keratoderma
\Functional finding\Hearing finding\Hearing disorder (disorder)\Hearing loss\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Mutilating keratoderma
\Functional finding\Abnormal keratinization\Rough skin (finding)\Rough skin of hands (finding)\Mutilating keratoderma
\Functional finding\Abnormal keratinization\Disorder of keratinisation\Inherited disorder of keratinisation\Erythrokeratoderma\Mutilating keratoderma

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Erythrokeratoderma\Mutilating keratoderma
\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Integumentary system finding\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Erythrokeratoderma\Mutilating keratoderma
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Keratoderma (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Disorder of skin of lower limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Disorder of skin of upper limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Integumentary system finding\Skin finding\Rough skin (finding)\Rough skin of hands (finding)\Mutilating keratoderma
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Keratoderma (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Disorder of skin of lower limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Disorder of skin of upper limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Integumentary system finding\Abnormal keratinization\Rough skin (finding)\Rough skin of hands (finding)\Mutilating keratoderma
\Integumentary system finding\Abnormal keratinization\Disorder of keratinisation\Inherited disorder of keratinisation\Erythrokeratoderma\Mutilating keratoderma

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Erythrokeratoderma\Mutilating keratoderma
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Auditory system hereditary disorder\Mutilating keratoderma
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Mutilating keratoderma
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Mutilating keratoderma
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Erythrokeratoderma\Mutilating keratoderma
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Auditory system hereditary disorder\Mutilating keratoderma
\Disease\Disorder of body system\Disorder of auditory system\Auditory system hereditary disorder\Mutilating keratoderma
\Disease\Disorder of body system\Disorder of auditory system\Hearing disorder (disorder)\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Mutilating keratoderma
\Disease\Disorder of body system\Disorder of auditory system\Hearing disorder (disorder)\Hearing loss\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Mutilating keratoderma
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Erythrokeratoderma\Mutilating keratoderma
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument (disorder)\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of body system\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Erythrokeratoderma\Mutilating keratoderma
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Keratoderma (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Disorder of skin of lower limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Disorder of skin of upper limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Keratosis (disorder)\Keratoderma (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of limb\Disorder of soft tissue of limb\Disorder of soft tissue of lower limb\Disorder of skin of lower limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of limb\Disorder of soft tissue of limb\Disorder of soft tissue of upper limb\Disorder of skin of upper limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of limb\Disorder of upper limb (disorder)\Disorder of soft tissue of upper limb\Disorder of skin of upper limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of limb\Disorder of upper limb (disorder)\Disorder of hand (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of limb\Disorder of lower limb\Disorder of free lower limb (disorder)\Disorder of foot (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of limb\Disorder of lower limb\Disorder of soft tissue of lower limb\Disorder of skin of lower limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of soft tissue\Disorder of soft tissue of limb\Disorder of soft tissue of lower limb\Disorder of skin of lower limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of soft tissue\Disorder of soft tissue of limb\Disorder of soft tissue of upper limb\Disorder of skin of upper limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Keratoderma (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Disorder of skin of lower limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Disorder of skin of upper limb (disorder)\Palmoplantar keratoderma\Hereditary palmoplantar keratoderma\Mutilating keratoderma

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Mutilating keratoderma	Is a	Congenital keratoderma	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Mutilating keratoderma	Is a	Hereditary palmoplantar keratoderma	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Mutilating keratoderma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Mutilating keratoderma	Associated morphology	Hyperkeratosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Mutilating keratoderma	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Mutilating keratoderma	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Mutilating keratoderma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Mutilating keratoderma	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Mutilating keratoderma	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Mutilating keratoderma	Associated morphology	Hyperkeratosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Mutilating keratoderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Mutilating keratoderma	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mutilating keratoderma	Interprets	Keratinisation	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mutilating keratoderma	Associated morphology	Hyperkeratosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Mutilating keratoderma	Finding site	Skin structure of palmar area of hand	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Mutilating keratoderma	Finding site	Skin structure of sole of foot (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Mutilating keratoderma	Is a	Rough skin of hands (finding)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Mutilating keratoderma	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Mutilating keratoderma	Is a	Erythrokeratoderma	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Mutilating keratoderma	Is a	Auditory system hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Mutilating keratoderma	Is a	Congenital sensorineural hearing loss (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Mutilating keratoderma	Interprets	Hearing	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Mutilating keratoderma	Has interpretation	Impaired (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Mutilating keratoderma	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Mutilating keratoderma	Finding site	Structure of auditory system (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	5

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Autosomal dominant mutilating keratoderma	Is a	False	Mutilating keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome is an inherited epidermal disorder characterised by palmoplantar keratoderma, linear hyperkeratotic papules on the flexural side of large joints (cord-like distribution around wrists, in antecubital and popliteal folds), hyperkeratotic plaques (on neck, axillae, elbows, wrists, and knees), mild ichthyosiform scaling, and sclerotic constrictions around fingers that present flexural deformities.	Is a	False	Mutilating keratoderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Keratoderma hereditarium mutilans with ichthyosis syndrome	Is a	True	Mutilating 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
41186015	Mutilating keratoderma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
754208012	Mutilating keratoderma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1223673015	Vohwinkel's mutilating keratoderma	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4589802013	Keratoderma hereditarium mutilans	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4589803015	Mutilating keratoderma of Vohwinkel	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4589804014	Vohwinkel syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
41186015	Mutilating keratoderma	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
41186015	Mutilating keratoderma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
754208012	Mutilating keratoderma (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
754208012	Mutilating keratoderma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1223673015	Vohwinkel's mutilating keratoderma	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1223673015	Vohwinkel's mutilating keratoderma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1223673015	Vohwinkel's mutilating keratoderma	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4589802013	Keratoderma hereditarium mutilans	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4589803015	Mutilating keratoderma of Vohwinkel	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4589804014	Vohwinkel syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3381631001000114	Keratoderma hereditarium mutilans	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4469331000241118	kératodermie mutilante	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4469331000241118	kératodermie mutilante	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3381631001000114	Keratoderma hereditarium mutilans	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module