Application Version: 4.0.6.10
Content Version: 2024.07.12
Release Notes [PDF288KB]
User Guide [PDF6.08MB]
Code System Update Calendar
Contact Us
Subscribe
Related Links
- PHIN Vocabulary Services
- Quick Links / Mapping Tools
- External Standards Resources
- Message Guides
- Developer's Guide
- PHINVADS FHIR API
Downloads
- RCMT Quick Search
Code System Concept
Code System Concept Code | 239076000 |
Code System Concept Name | Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder) |
Code System Preferred Concept Name | Palmoplantar hyperkeratosis sclerodactyly 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Superseded By Concept | |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 |
---|---|---|---|---|---|
358285012 | Keratoderma with scleroatrophy of the extremities | Active | Synonym | false | false |
358286013 | Huriez syndrome | Active | Synonym | false | false |
4590597010 | Palmoplantar hyperkeratosis sclerodactyly syndrome | Active | Synonym | false | false |
4590598017 | Keratoderma with scleroatrophy of extremities | Active | Synonym | false | false |
4590599013 | Palmoplantar keratoderma sclerodactyly syndrome | Active | Synonym | false | false |
4590600011 | Scleroatrophic syndrome | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
Autosomal dominant hereditary disorder (disorder)
{11164009
, SNOMED-CT
}
Circumscribed palmoplantar keratoderma (disorder)
{239073008
, SNOMED-CT
}
Congenital abnormality of foot and toes (disorder)
{253966001
, SNOMED-CT
}
Congenital anomaly of hand (disorder)
{34111000
, SNOMED-CT
}
Congenital anomaly of skin (disorder)
{199879009
, SNOMED-CT
}
Congenital keratoderma (disorder)
{6874009
, SNOMED-CT
}
Developmental hereditary disorder (disorder)
{363070008
, SNOMED-CT
}
Hereditary diffuse palmoplantar keratoderma (disorder)
{400123002
, SNOMED-CT
}
Rough skin of hands (finding)
{829993001
, SNOMED-CT
}
|
Other Relationships
No other relationships present.
|
Child Concepts
No child concepts present.
|
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: