Application Version: 4.0.6.10
Content Version: 2024.07.12
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Code System Concept
Code System Concept Code | 367417005 |
Code System Concept Name | Propionyl-CoA carboxylase deficiency (disorder) |
Code System Preferred Concept Name | Propionyl-CoA carboxylase deficiency (disorder) |
Concept Status | Retired |
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Superseded By Concept |
Concept Code:
69080001
Concept Name: Propionic acidemia (disorder) Code System: SNOMED-CT |
SDO Concept Status | Inactive |
SDO Concept Status Date | 07/31/2002 |
SDO Date Created | 01/31/2002 |
SDO Date Revised | 07/31/2002 |
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 |
---|---|---|---|---|---|
2671104014 | Propionyl-CoA carboxylase deficiency [dup] | Active | Synonym | false | false |
2769729011 | Propionyl-CoA carboxylase deficiency | Active | Synonym | false | false |
491927011 | Propionic acidaemia, type I | Active | Synonym | false | false |
491928018 | Propionic acidaemia, type II | Active | Synonym | false | false |
491929014 | Hyperglycinaemia with ketosis and leucopenia, types I and II | Active | Synonym | false | false |
491930016 | Ketotic glycinaemia, types I and II | Active | Synonym | false | false |
491931017 | Propionic acidemia, type I | Active | Synonym | false | false |
491932012 | Hyperglycinemia with ketosis and leukopenia, types I and II | Active | Synonym | false | false |
491933019 | Ketotic glycinemia, types I and II | Active | Synonym | false | false |
491934013 | Propionic acidemia, type II | Active | Synonym | false | false |
491935014 | Propionyl-CoA carboxylase deficiency (disorder) | Active | Synonym | false | false |
Associated Value Sets
No associated value sets.
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
Autosomal recessive hereditary disorder (disorder)
{85995004
, SNOMED-CT
}
Congenital anomaly of the hematopoietic system (disorder)
{40888008
, SNOMED-CT
}
Enzymopathy (disorder)
{78548001
, SNOMED-CT
}
Hereditary disorder of hematologic system (disorder)
{363136009
, SNOMED-CT
}
Hyperglycinemia (disorder)
{64654004
, SNOMED-CT
}
Leukopenia (disorder)
{84828003
, SNOMED-CT
}
Propionic acidemia (disorder)
{69080001
, SNOMED-CT
}
|
Other Relationships
No other relationships present.
|
Child Concepts
Propionyl-CoA carboxylase deficiency (disorder) {367417005 , SNOMED-CT } |
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: