Application Version: 4.0.6.10
Content Version: 2024.07.12
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Code System Concept
Code System Concept Code | 718749004 |
Code System Concept Name | Generalized peeling skin syndrome (disorder) |
Code System Preferred Concept Name | Generalized peeling skin syndrome (disorder) |
Concept Status | Published |
Concept Status Date | 09/01/2024 |
Code System Name | SNOMED-CT |
Concept Details
Code System Code | PH_SNOMED-CT |
Code System OID | 2.16.840.1.113883.6.96 |
HL7 Table 0396 Code | SCT |
Superseded By Concept | |
SDO Concept Status | Active |
SDO Concept Status Date | 01/31/2017 |
SDO Date Created | 01/31/2017 |
SDO Date Revised | 01/31/2017 |
Description | A form of peeling skin syndrome that presents with a generalised distribution. It comprises two sub-types: the non-inflammatory (PSS type A) and the inflammatory (PSS type B) forms. |
Sequence |
Extended Properties
No extended properties.
Concept Alternate Designations
SDO Designation ID | Concept Designation Description | Status | Designation Type | PHIN Preferred Term Flag | Code Flag |
---|---|---|---|---|---|
3313721014 | Generalized peeling skin syndrome | Active | Synonym | false | false |
3313722019 | Generalised peeling skin syndrome | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
Autosomal recessive hereditary disorder (disorder)
{85995004
, SNOMED-CT
}
Hereditary disorder of the integument (disorder)
{363185004
, SNOMED-CT
}
Hereditary skin peeling syndrome (disorder)
{724838009
, SNOMED-CT
}
Inherited disorder of keratinization (disorder)
{254214009
, SNOMED-CT
}
Skin peeling disorder (disorder)
{238643009
, SNOMED-CT
}
|
Other Relationships
No other relationships present.
|
Child Concepts
Generalized peeling skin syndrome (disorder) {718749004 , SNOMED-CT } |
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: