Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3643764019 | Autosomal recessive exfoliative ichthyosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3643765018 | Ichthyosis exfoliativa | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3643766017 | Autosomal recessive exfoliative ichthyosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3643767014 | Exfoliative ichthyosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3643768016 | An inherited non-syndromic congenital ichthyosis characterised by the infancy-onset of palmoplantar peeling of the skin (aggravated by exposure to water and by occlusion) associated with dry, scaly skin over most of the body. Pruritus and hypohidrosis may also be associated. Well-demarcated areas of denuded skin appear in moist and traumatised regions and skin biopsies reveal reduced cell-cell adhesion in the basal and suprabasal layers, prominent intercellular oedema, numerous aggregates of keratin filaments in basal keratinocytes, attenuated cornified cell envelopes, and epidermal barrier impairment. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3643769012 | An inherited non-syndromic congenital ichthyosis characterized by the infancy-onset of palmoplantar peeling of the skin (aggravated by exposure to water and by occlusion) associated with dry, scaly skin over most of the body. Pruritus and hypohidrosis may also be associated. Well-demarcated areas of denuded skin appear in moist and traumatized regions and skin biopsies reveal reduced cell-cell adhesion in the basal and suprabasal layers, prominent intercellular edema, numerous aggregates of keratin filaments in basal keratinocytes, attenuated cornified cell envelopes, and epidermal barrier impairment. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
9985691000172116 | ichtyose exfoliative autosomique récessive | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4279091000172119 | autosomaal recessieve ichthyosis exfoliativa | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4279101000172110 | autosomaal recessieve exfoliatieve ichtyose | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4279111000172113 | autosomaal recessieve ichthyosis bullosa van Siemens | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive exfoliative ichthyosis (disorder) | Is a | Autosomal recessive ichthyosis (disorder) | true | Inferred relationship | Some | ||
Autosomal recessive exfoliative ichthyosis (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 1 | |
Autosomal recessive exfoliative ichthyosis (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal recessive exfoliative ichthyosis (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Autosomal recessive exfoliative ichthyosis (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive exfoliative ichthyosis (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Autosomal recessive exfoliative ichthyosis (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Autosomal recessive exfoliative ichthyosis (disorder) | Interprets | Keratinization | true | Inferred relationship | Some | 2 | |
Autosomal recessive exfoliative ichthyosis (disorder) | Finding site | Entire skin | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets