Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1001371000172112 | syndrome de dermatite sévère-allergies multiples-cachexie métabolique | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3728377017 | Severe dermatitis, multiple allergies, metabolic wasting syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3728378010 | Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3728379019 | Congenital erythroderma, hypotrichosis, recurrent infections, multiple food allergies syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3728380016 | SAM syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 772421000241114 | syndrome de dermatite sévère-allergies multiples-cachexie métabolique (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 984301000172110 | syndrome SAM | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3728381017 | A rare genetic epidermal disorder with characteristics of congenital erythroderma with severe psoriasiform dermatitis, ichthyosis, severe palmoplantar keratoderma, yellow keratosis on the hands and feet, elevated immunoglobulin E, multiple food allergies, and metabolic wasting. Other variable features may include hypotrichosis, nail dystrophy, recurrent infections, mild global developmental delay, eosinophilia, nystagmus, growth impairment and cardiac defects. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | Combined immunodeficiency disease | true | Inferred relationship | Some | ||
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | Congenital immunodeficiency disease | true | Inferred relationship | Some | ||
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | Hereditary disorder of immune system | true | Inferred relationship | Some | ||
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | morphologie associée (attribut) | Diffuse inflammation | true | Inferred relationship | Some | 1 | |
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | Congenital anomaly of skin | true | Inferred relationship | Some | ||
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | interprète (attribut) | Immunoglobulin E measurement | true | Inferred relationship | Some | 2 | |
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | Erythroderma (disorder) | true | Inferred relationship | Some | ||
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | Increased immunoglobulin | true | Inferred relationship | Some | ||
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | localisation d'une constatation (attribut) | structure de la peau | true | Inferred relationship | Some | 1 | |
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | a pour interprétation (attribut) | au-dessus de l'étendue de référence | true | Inferred relationship | Some | 2 | |
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 4 | |
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | localisation d'une constatation (attribut) | structure de la peau | true | Inferred relationship | Some | 3 | |
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | morphologie associée (attribut) | érythème (anomalie morphologique) | true | Inferred relationship | Some | 3 | |
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | Diffuse dermatitis (disorder) | true | Inferred relationship | Some | ||
| syndrome de dermatite sévère-allergies multiples-cachexie métabolique | est un(e) (attribut) | Developmental hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR