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367417005: Propionyl-CoA carboxylase deficiency (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2002. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    491927011 Propionic acidaemia, type I en Synonym Active Only initial character case insensitive SNOMED CT core module
    491928018 Propionic acidaemia, type II en Synonym Active Only initial character case insensitive SNOMED CT core module
    491929014 Hyperglycinaemia with ketosis and leucopenia, types I and II en Synonym Active Only initial character case insensitive SNOMED CT core module
    491930016 Ketotic glycinaemia, types I and II en Synonym Active Only initial character case insensitive SNOMED CT core module
    491931017 Propionic acidemia, type I en Synonym Active Only initial character case insensitive SNOMED CT core module
    491932012 Hyperglycinemia with ketosis and leukopenia, types I and II en Synonym Active Only initial character case insensitive SNOMED CT core module
    491933019 Ketotic glycinemia, types I and II en Synonym Active Only initial character case insensitive SNOMED CT core module
    491934013 Propionic acidemia, type II en Synonym Active Only initial character case insensitive SNOMED CT core module
    2741499010 Propionyl-CoA carboxylase deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
    2769729011 Propionyl-CoA carboxylase deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Propionyl-CoA carboxylase deficiency Is a Hereditary disorder of hematologic system false Inferred relationship Existential restriction modifier
    Propionyl-CoA carboxylase deficiency Is a Leukopenia false Inferred relationship Existential restriction modifier
    Propionyl-CoA carboxylase deficiency Is a Hyperglycinemia false Inferred relationship Existential restriction modifier
    Propionyl-CoA carboxylase deficiency Is a Propionic acidemia false Inferred relationship Existential restriction modifier
    Propionyl-CoA carboxylase deficiency Is a Congenital anomaly of the hematopoietic system 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
    Propionyl-CoA carboxylase deficiency Finding site Leukocyte false Inferred relationship Existential restriction modifier
    Propionyl-CoA carboxylase deficiency Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
    Propionyl-CoA carboxylase deficiency Occurrence Congenital 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

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