Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3308724010 | X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3308725011 | X-linked reticulate pigmentary disorder with systemic manifestation syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3308726012 | Partington disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3308727015 | An extremely rare skin disease described in only four families to date and characterized in males by diffuse reticulate brown hyperpigmented skin lesions developing in early childhood and a variety of systemic manifestations (recurrent pneumonia, corneal opacification, gastrointestinal inflammation, urethral stricture, failure to thrive, hypohidrosis, digital clubbing, and unruly hair and flared eyebrows), while in females, there is only cutaneous involvement with the development in early childhood of localized brown hyperpigmented skin lesions following the lines of Blaschko. This disease was first considered as a cutaneous amyloidosis, but amyloid deposits are an inconstant feature. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3308728013 | An extremely rare skin disease described in only four families to date and characterised in males by diffuse reticulate brown hyperpigmented skin lesions developing in early childhood and a variety of systemic manifestations (recurrent pneumonia, corneal opacification, gastrointestinal inflammation, urethral stricture, failure to thrive, hypohidrosis, digital clubbing, and unruly hair and flared eyebrows), while in females, there is only cutaneous involvement with the development in early childhood of localised brown hyperpigmented skin lesions following the lines of Blaschko. This disease was first considered as a cutaneous amyloidosis, but amyloid deposits are an inconstant feature. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 1 | |
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | morphologie associée (attribut) | Hyperpigmentation (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | est un(e) (attribut) | X-linked dominant hereditary disease (disorder) | true | Inferred relationship | Some | ||
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | est un(e) (attribut) | hyperpigmentation de la peau | true | Inferred relationship | Some | ||
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | est un(e) (attribut) | X-linked hereditary disease | false | Inferred relationship | Some | ||
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | est un(e) (attribut) | Inherited cutaneous hyperpigmentation | false | Inferred relationship | Some | ||
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | est un(e) (attribut) | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 2 | |
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 3 | |
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | morphologie associée (attribut) | Hyperpigmentation (morphologic abnormality) | false | Inferred relationship | Some | 2 | |
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | morphologie associée (attribut) | Developmental abnormality | false | Inferred relationship | Some | 3 | |
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 3 | |
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | est un(e) (attribut) | Genetic disorder of skin pigmentation (disorder) | true | Inferred relationship | Some | ||
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | localisation d'une constatation (attribut) | structure de la peau | true | Inferred relationship | Some | 1 | |
| X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
Description inactivation indicator reference set
FHIR