367417005: Propionyl-CoA carboxylase deficiency (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

491927011 Propionic acidaemia, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

491928018 Propionic acidaemia, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

491929014 Hyperglycinaemia with ketosis and leucopenia, types I and II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

491930016 Ketotic glycinaemia, types I and II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

491931017 Propionic acidemia, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

491932012 Hyperglycinemia with ketosis and leukopenia, types I and II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

491933019 Ketotic glycinemia, types I and II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

491934013 Propionic acidemia, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2741499010 Propionyl-CoA carboxylase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2769729011 Propionyl-CoA carboxylase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Propionyl-CoA carboxylase deficiency	Is a	Hereditary disorder of hematologic system	false	Inferred relationship	Some
Propionyl-CoA carboxylase deficiency	Is a	Leucopenia	false	Inferred relationship	Some
Propionyl-CoA carboxylase deficiency	Is a	Hyperglycinemia	false	Inferred relationship	Some
Propionyl-CoA carboxylase deficiency	Is a	Propionic acidemia	false	Inferred relationship	Some
Propionyl-CoA carboxylase deficiency	Is a	Congenital anomaly of the hematopoietic system	false	Inferred relationship	Some
Propionyl-CoA carboxylase deficiency	Is a	Autosomal recessive hereditary disorder	false	Inferred relationship	Some
Propionyl-CoA carboxylase deficiency	Is a	Enzymopathy	false	Inferred relationship	Some
Propionyl-CoA carboxylase deficiency	Finding site	Leukocyte	false	Inferred relationship	Some
Propionyl-CoA carboxylase deficiency	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Propionyl-CoA carboxylase deficiency	Occurrence	Congenital	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Propionyl-CoA carboxylase deficiency pccA complementation group	Is a	False	Propionyl-CoA carboxylase deficiency	Inferred relationship	Some
Propionyl-coenzyme A carboxylase deficiency pccBC complementation group (disorder)	Is a	False	Propionyl-CoA carboxylase deficiency	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

Description inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)