Status: current, Primitive. 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 | Case insensitive | SNOMED CT core |
3643765018 | Ichthyosis exfoliativa | en | Synonym | Active | Case insensitive | SNOMED CT core |
3643766017 | Autosomal recessive exfoliative ichthyosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3643767014 | Exfoliative ichthyosis | en | Synonym | Active | Case insensitive | 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 | Case sensitive | 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 | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive exfoliative ichthyosis | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive exfoliative ichthyosis | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Autosomal recessive exfoliative ichthyosis | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Autosomal recessive exfoliative ichthyosis | Interprets | Keratinisation | true | Inferred relationship | Some | 2 | |
Autosomal recessive exfoliative ichthyosis | Finding site | Entire skin | true | Inferred relationship | Some | 1 | |
Autosomal recessive exfoliative ichthyosis | Is a | Autosomal recessive ichthyosis | true | Inferred relationship | Some | ||
Autosomal recessive exfoliative ichthyosis | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
Autosomal recessive exfoliative ichthyosis | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal recessive exfoliative ichthyosis | Finding site | Skin structure | false | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set