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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
    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


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Propionyl-CoA carboxylase deficiency est un(e) (attribut) Autosomal recessive hereditary disorder false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency est un(e) (attribut) Enzymopathy false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency est un(e) (attribut) Disorder of branched-chain amino acid metabolism false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency survenue (attribut) congénital false Inferred relationship Some

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

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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