Application Version: 4.0.6.10
Content Version: 2024.07.12
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Code System Concept
| Code System Concept Code | 7731005 |
| Code System Concept Name | Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) |
| Code System Preferred Concept Name | Autosomal dominant hypohidrotic ectodermal dysplasia 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| Superseded By Concept | |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 | 01/31/2002 |
| SDO Date Created | 01/31/2002 |
| SDO Date Revised | 01/31/2002 |
| Description | |
| Sequence |
Extended Properties
No extended properties.
Concept Alternate Designations
| SDO Designation ID | Concept Designation Description | Status | Designation Type | PHIN Preferred Term Flag | Code Flag |
|---|---|---|---|---|---|
| 13786011 | Autosomal dominant hypohidrotic ectodermal dysplasia syndrome | Active | Synonym | false | false |
| 13787019 | Rapp-Hodgkin ectodermal dysplasia syndrome | Active | Synonym | false | false |
| 503512017 | Anhidrotic ectodermal dysplasia | Active | Synonym | false | false |
| 503513010 | Rapp-Hodgkin type of ectodermal dysplasia | Active | Synonym | false | false |
| 503514016 | Hypohidrotic ectodermal dysplasia | Active | Synonym | false | false |
| 503515015 | Anhidrotic ectodermal dysplasia syndrome | Active | Synonym | false | false |
| 503516019 | Hypohidrotic ectodermal dysplasia syndrome | Active | Synonym | false | false |
|
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
Autosomal dominant hereditary disorder (disorder)
{11164009
, SNOMED-CT
}
Developmental hereditary disorder (disorder)
{363070008
, SNOMED-CT
}
Digestive system hereditary disorder (disorder)
{363080007
, SNOMED-CT
}
Ectodermal dysplasia with hair-tooth-nail-sweating defect (disorder)
{239006001
, SNOMED-CT
}
Genetic disorder of nail (disorder)
{402775007
, SNOMED-CT
}
Hereditary disorder of the integument (disorder)
{363185004
, SNOMED-CT
}
Hereditary disorder of tooth (disorder)
{1148766007
, SNOMED-CT
}
Skin lesion (disorder)
{95324001
, SNOMED-CT
}
|
Other Relationships
No other relationships present.
|
|
Child Concepts
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) {7731005 , SNOMED-CT }
Parent/Child (Relationship Type)
|
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: