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360364008: Propionyl-CoA carboxylase deficiency (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    476080015 PCC - Propionyl-CoA carboxylase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    476081016 Hyperglycinemia with ketosis AND leukopenia, types I AND/OR II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    476082011 Propionyl-CoA carboxylase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    476083018 Hyperglycinaemia with ketosis AND leucopenia, types I AND/OR II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    740018011 Propionyl-CoA carboxylase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1216455017 Propionic acidaemia, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1216456016 Ketotic glycinaemia, types I and II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1216457013 Propionic acidaemia, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1216458015 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
    1217945017 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
    1217946016 Propionic acidemia, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1217947013 Propionic acidemia, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1217948015 Ketotic glycinemia, types I and II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    476080015 PCC - Propionyl-CoA carboxylase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    476081016 Hyperglycinemia with ketosis AND leukopenia, types I AND/OR II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    476082011 Propionyl-CoA carboxylase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    476083018 Hyperglycinaemia with ketosis AND leucopenia, types I AND/OR II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    740018011 Propionyl-CoA carboxylase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1216455017 Propionic acidaemia, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1216456016 Ketotic glycinaemia, types I and II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1216457013 Propionic acidaemia, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1216458015 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
    1217945017 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
    1217946016 Propionic acidemia, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1217947013 Propionic acidemia, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1217948015 Ketotic glycinemia, types I and II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    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 (core metadata concept)
    Propionyl-CoA carboxylase deficiency Finding site Body 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)
    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)
    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

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