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 |
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)