Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3008765012 | Congenital reticular ichthyosiform erythroderma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3008789017 | Congenital reticular ichthyosiform erythroderma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3008812013 | Ichthyosis with confetti | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3008838013 | Ichthyosis variegata | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3008848010 | CRIE - Congenital reticular ichthyosiform erythroderma | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital reticular ichthyosiform erythroderma (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Congenital reticular ichthyosiform erythroderma (disorder) | Is a | Congenital ichthyosiform erythroderma | true | Inferred relationship | Some | ||
| Congenital reticular ichthyosiform erythroderma (disorder) | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
| Congenital reticular ichthyosiform erythroderma (disorder) | Has definitional manifestation | Abnormal keratinization | false | Inferred relationship | Some | ||
| Congenital reticular ichthyosiform erythroderma (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Congenital reticular ichthyosiform erythroderma (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
| Congenital reticular ichthyosiform erythroderma (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
| Congenital reticular ichthyosiform erythroderma (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
| Congenital reticular ichthyosiform erythroderma (disorder) | Finding site | Structure of integumentary system (body structure) | false | Inferred relationship | Some | ||
| Congenital reticular ichthyosiform erythroderma (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Congenital reticular ichthyosiform erythroderma (disorder) | Interprets | Keratinization | true | Inferred relationship | Some | 1 | |
| Congenital reticular ichthyosiform erythroderma (disorder) | Finding site | Structure of integumentary system (body structure) | true | Inferred relationship | Some | 2 | |
| Congenital reticular ichthyosiform erythroderma (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR