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:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Propionyl-CoA carboxylase deficiency	Is a	Hereditary disorder of haematologic sysem	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency	Is a	Leucopenia	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency	Is a	Hyperglycinemia	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency	Is a	Propionic acidemia (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency	Is a	Congenital anomaly of the haematopoietic system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency	Is a	Autosomal recessive hereditary disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency	Is a	Enzymopathy	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency	Finding site	Leucocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)

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

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set

SAME AS association reference set (foundation metadata concept)

Back to Start

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
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
491935014	Propionyl-CoA carboxylase deficiency (disorder)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
775490017	Propionyl-CoA carboxylase deficiency [dup] (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2671104014	Propionyl-CoA carboxylase deficiency [dup]	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