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 | 59763006 |
Code System Concept Name | Hyperphosphatasemia tarda (disorder) |
Code System Preferred Concept Name | Hyperphosphatasemia tarda (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Superseded By Concept | |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 |
---|---|---|---|---|---|
498533016 | Endosteal hyperostosis | Active | Synonym | false | false |
498534010 | Van Buchem disease | Active | Synonym | false | false |
498535011 | Hyperphosphatasaemia tarda | Active | Synonym | false | false |
99274013 | Hyperphosphatasemia tarda | Active | Synonym | false | false |
99275014 | Hyperostosis corticalis generalisata | Active | Synonym | false | false |
99276010 | Leontiasis ossea generalisata | Active | Synonym | false | false |
99277018 | Hyperphosphatasia tarda | Active | Synonym | false | false |
99278011 | van Buchem's syndrome | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
Congenital anomaly of cartilage (disorder)
{67988000
, SNOMED-CT
}
Congenital anomaly of face (disorder)
{75901008
, SNOMED-CT
}
Congenital anomaly of integument (disorder)
{38164009
, SNOMED-CT
}
Congenital anomaly of skull (disorder)
{51655004
, SNOMED-CT
}
Congenital bacterial disorder (disorder)
{363038008
, SNOMED-CT
}
Endosteal hyperostoses (disorder)
{254130008
, SNOMED-CT
}
Exostosis (disorder)
{416189003
, SNOMED-CT
}
Hypertrophy of bone (disorder)
{203514008
, SNOMED-CT
}
Leontiasis ossium (disorder)
{16442005
, SNOMED-CT
}
Metabolic bone disease (disorder)
{50279003
, 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: