Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4011667017 | Autosomal recessive epidermolytic ichthyosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4011668010 | Autosomal recessive epidermolytic ichthyosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive epidermolytic ichthyosis (disorder) | Is a | Autosomal recessive ichthyosis (disorder) | true | Inferred relationship | Some | ||
Autosomal recessive epidermolytic ichthyosis (disorder) | Is a | Keratinopathic ichthyosis (disorder) | true | Inferred relationship | Some | ||
Autosomal recessive epidermolytic ichthyosis (disorder) | Finding site | Entire skin | true | Inferred relationship | Some | 1 | |
Autosomal recessive epidermolytic ichthyosis (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal recessive epidermolytic ichthyosis (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive epidermolytic ichthyosis (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Autosomal recessive epidermolytic ichthyosis (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Autosomal recessive epidermolytic ichthyosis (disorder) | Interprets | Keratinization | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets