360364008: Propionyl-CoA carboxylase deficiency (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

476080015 PCC - Propionyl-CoA carboxylase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module

476081016 Hyperglycinemia with ketosis AND leukopenia, types I AND/OR II en Synonym Active Only initial character case insensitive SNOMED CT core module

476082011 Propionyl-CoA carboxylase deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module

476083018 Hyperglycinaemia with ketosis AND leucopenia, types I AND/OR II en Synonym Active Only initial character case insensitive SNOMED CT core module

740018011 Propionyl-CoA carboxylase deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

1216455017 Propionic acidaemia, type I en Synonym Active Only initial character case insensitive SNOMED CT core module

1216456016 Ketotic glycinaemia, types I and II en Synonym Active Only initial character case insensitive SNOMED CT core module

1216457013 Propionic acidaemia, type II en Synonym Active Only initial character case insensitive SNOMED CT core module

1216458015 Hyperglycinaemia with ketosis and leucopenia, types I and II en Synonym Active Only initial character case insensitive SNOMED CT core module

1217945017 Hyperglycinemia with ketosis and leukopenia, types I and II en Synonym Active Only initial character case insensitive SNOMED CT core module

1217946016 Propionic acidemia, type I en Synonym Active Only initial character case insensitive SNOMED CT core module

1217947013 Propionic acidemia, type II en Synonym Active Only initial character case insensitive SNOMED CT core module

1217948015 Ketotic glycinemia, types I and II en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Propionyl-CoA carboxylase deficiency	Is a	Disorder of branched-chain amino acid metabolism	false	Inferred relationship	Existential restriction modifier
Propionyl-CoA carboxylase deficiency	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Propionyl-CoA carboxylase deficiency	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Propionyl-CoA carboxylase deficiency	Is a	Autosomal recessive hereditary disorder	false	Inferred relationship	Existential restriction modifier
Propionyl-CoA carboxylase deficiency	Is a	Enzymopathy	false	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Propionyl-coenzyme A carboxylase deficiency pccA complementation group	Is a	False	Propionyl-CoA carboxylase deficiency	Inferred relationship	Existential restriction modifier
Propionyl-coenzyme A carboxylase deficiency pccBC complementation group	Is a	False	Propionyl-CoA carboxylase deficiency	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets