Application Version: 4.0.6.10
Content Version: 2024.07.12
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Code System Concept
Code System Concept Code | 234571003 |
Code System Concept Name | Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder) |
Code System Preferred Concept Name | Warts, hypogammaglobulinemia, infections, and myelokathexis (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Superseded By Concept | |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 |
---|---|---|---|---|---|
351461010 | WHIM - Warts, hypogammaglobulinaemia, infections and myelokathexis | Active | Synonym | false | false |
351462015 | WHIM - Warts, hypogammaglobulinemia, infections and myelokathexis | Active | Synonym | false | false |
351463013 | Warts, hypogammaglobulinaemia, infections, and myelokathexis | Active | Synonym | false | false |
351464019 | Warts, hypogammaglobulinemia, infections, and myelokathexis | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
Congenital neutropenia (disorder)
{89655007
, SNOMED-CT
}
Disorder of immune structure (disorder)
{414030009
, SNOMED-CT
}
Hereditary white blood cell disorder (disorder)
{414395005
, SNOMED-CT
}
Myelokathexis (disorder)
{24974008
, SNOMED-CT
}
Severe combined immunodeficiency disease (disorder)
{31323000
, 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: