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360364008: Propionyl-CoA carboxylase deficiency (disorder)

    Status: retired, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

    Descriptions:

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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    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 Is a Disorder of branched-chain amino acid metabolism false Inferred relationship Some
    Propionyl-CoA carboxylase deficiency Finding site Body 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-CoA carboxylase deficiency pccBC complementation group Is a False Propionyl-CoA carboxylase deficiency Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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