Code System Concept

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Code System Concept

Code System Concept Code	360364008
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 Relationships
Concept Details

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Superseded By Concept	Concept Code: 69080001 Concept Name: Propionic acidemia (disorder) Code System: SNOMED-CT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	07/31/2003
SDO Date Created	01/31/2002
SDO Date Revised	07/31/2003
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
1216455017	Propionic acidaemia, type I	Active	Synonym	false	false
1216456016	Ketotic glycinaemia, types I and II	Active	Synonym	false	false
1216457013	Propionic acidaemia, type II	Active	Synonym	false	false
1216458015	Hyperglycinaemia with ketosis and leucopenia, types I and II	Active	Synonym	false	false
1217945017	Hyperglycinemia with ketosis and leukopenia, types I and II	Active	Synonym	false	false
1217946016	Propionic acidemia, type I	Active	Synonym	false	false
1217947013	Propionic acidemia, type II	Active	Synonym	false	false
1217948015	Ketotic glycinemia, types I and II	Active	Synonym	false	false
476080015	PCC - Propionyl-CoA carboxylase deficiency	Active	Synonym	false	false
476081016	Hyperglycinemia with ketosis AND leukopenia, types I AND/OR II	Active	Synonym	false	false
476082011	Propionyl-CoA carboxylase deficiency	Active	Synonym	false	false
476083018	Hyperglycinaemia with ketosis AND leucopenia, types I AND/OR II	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 } Disorder of branched-chain amino acid metabolism (disorder) {116020001 , SNOMED-CT } Enzymopathy (disorder) {78548001 , SNOMED-CT }	Other Relationships No other relationships present.
Child Concepts Propionyl-CoA carboxylase deficiency (disorder) {360364008 , SNOMED-CT } Parent/Child (Relationship Type) Propionyl-coenzyme A carboxylase deficiency pccA complementation group (disorder) {303094000 , SNOMED-CT } Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder) {303095004 , SNOMED-CT }

Page last reviewed:June 20, 2024
Page last updated:June 20, 2024
Content source:
- Centers for Disease Control and Prevention,