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724838009: Hereditary skin peeling syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3449166014 Hereditary skin peeling syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3449167017 Hereditary skin peeling syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4594936015 Peeling skin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4594937012 Familial continuous skin peeling syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5403346017 A group of rare autosomal recessive forms of ichthyosis clinically characterized by superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. PSS presents with either an acral (acral PSS) or a generalized distribution for generalized PSS type A (noninflammatory) or B (inflammatory). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403347014 A group of rare autosomal recessive forms of ichthyosis clinically characterised by superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. PSS presents with either an acral (acral PSS) or a generalised distribution for generalised PSS type A (noninflammatory) or B (inflammatory). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3449166014 Hereditary skin peeling syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3449167017 Hereditary skin peeling syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4594936015 Peeling skin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4594937012 Familial continuous skin peeling syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4594934017 A group of rare autosomal recessive forms of ichthyosis with clinical characteristics of superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. Presents with either an acral or a generalised distribution. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4594935016 A group of rare autosomal recessive forms of ichthyosis with clinical characteristics of superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. Presents with either an acral or a generalized distribution. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403346017 A group of rare autosomal recessive forms of ichthyosis clinically characterized by superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. PSS presents with either an acral (acral PSS) or a generalized distribution for generalized PSS type A (noninflammatory) or B (inflammatory). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403347014 A group of rare autosomal recessive forms of ichthyosis clinically characterised by superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. PSS presents with either an acral (acral PSS) or a generalised distribution for generalised PSS type A (noninflammatory) or B (inflammatory). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3427541001000111 Peeling Skin-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246471000241119 syndrome héréditaire de desquamation cutanée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246481000241117 syndrome héréditaire de desquamation de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246471000241119 syndrome héréditaire de desquamation cutanée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246481000241117 syndrome héréditaire de desquamation de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3427541001000111 Peeling Skin-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary skin peeling syndrome (disorder) Is a Skin peeling disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary skin peeling syndrome (disorder) Is a Inherited disorder of keratinisation false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary skin peeling syndrome (disorder) Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary skin peeling syndrome (disorder) Associated morphology Exfoliative lesion true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary skin peeling syndrome (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary skin peeling syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary skin peeling syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary skin peeling syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary skin peeling syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary skin peeling syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary skin peeling syndrome (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary skin peeling syndrome (disorder) Interprets Keratinisation true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary skin peeling syndrome (disorder) Is a Developmental hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary skin peeling syndrome (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary skin peeling syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary skin peeling syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary skin peeling syndrome (disorder) Is a Autosomal recessive ichthyosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary skin peeling syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary skin peeling syndrome (disorder) Finding site Entire skin true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary skin peeling syndrome (disorder) Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary skin peeling syndrome (disorder) 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
Generalized peeling skin syndrome (disorder) Is a True Hereditary skin peeling syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Acral peeling skin syndrome Is a True Hereditary skin peeling syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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