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709416009: Acral peeling skin syndrome (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane (disorder)\Skin lesion\Skin peeling disorder\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Rough skin (finding)\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Keratoderma (disorder)\Ichthyosis (disorder)\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Genodermatosis\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Skin lesion\Skin peeling disorder\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome

\General finding of soft tissue\Skin finding\Rough skin (finding)\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Keratoderma (disorder)\Ichthyosis (disorder)\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Genodermatosis\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Skin lesion\Skin peeling disorder\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\General finding of soft tissue\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Skin peeling disorder\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Keratoderma (disorder)\Ichthyosis (disorder)\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Genodermatosis\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Skin peeling disorder\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome

\Functional finding\Abnormal keratinization\...

\Rough skin (finding)\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome

\Disorder of keratinisation\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Disorder of keratinisation\Skin peeling disorder\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Disorder of integument\Disorder of keratinisation\Skin peeling disorder\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Disorder of integument\Disorder involving the integument of fetus OR newborn\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Genodermatosis\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Keratoderma (disorder)\Ichthyosis (disorder)\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Genodermatosis\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Skin peeling disorder\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Skin finding\Rough skin (finding)\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Keratoderma (disorder)\Ichthyosis (disorder)\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Genodermatosis\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Skin lesion\Skin peeling disorder\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Abnormal keratinization\Rough skin (finding)\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Abnormal keratinization\Disorder of keratinisation\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Autosomal recessive ichthyosis (disorder)\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome
\Integumentary system finding\Abnormal keratinization\Disorder of keratinisation\Skin peeling disorder\Hereditary skin peeling syndrome (disorder)\Acral peeling skin syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Acral peeling skin syndrome	Is a	Hereditary disorder of the integument (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Acral peeling skin syndrome	Is a	Autosomal recessive hereditary disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Acral peeling skin syndrome	Is a	Skin peeling disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Acral peeling skin syndrome	Has definitional manifestation	Abnormal keratinization	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Acral peeling skin syndrome	Is a	Inherited disorder of keratinisation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Acral peeling skin syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Acral peeling skin syndrome	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Acral peeling skin syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Acral peeling skin syndrome	Associated morphology	Exfoliative lesion	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Acral peeling skin syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Acral peeling skin syndrome	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acral peeling skin syndrome	Interprets	Keratinisation	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acral peeling skin syndrome	Is a	Hereditary skin peeling syndrome (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Acral peeling skin syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acral peeling skin syndrome	Finding site	Entire skin	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acral peeling skin syndrome	Associated morphology	Hyperkeratosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acral peeling skin syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3039903018	Peeling skin syndrome, acral type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3040122019	Acral peeling skin syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3040206011	Acral peeling skin syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3039903018	Peeling skin syndrome, acral type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3039903018	Peeling skin syndrome, acral type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3040122019	Acral peeling skin syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3040122019	Acral peeling skin syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3040206011	Acral peeling skin syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3040206011	Acral peeling skin syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3394341001000112	Peeling-Skin-Syndrom, lokalisiertes	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
979551000172111	peeling skin syndrome type acral	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
996261000172110	PSS acral - peeling skin syndrome type acral	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
979551000172111	peeling skin syndrome type acral	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
996261000172110	PSS acral - peeling skin syndrome type acral	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3394341001000112	Peeling-Skin-Syndrom, lokalisiertes	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module