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32053001: Acetyl-CoA: acyltransferase deficiency (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    485115016 3-Methylhydroxybutyric acidaemia en Synonym Active Case sensitive SNOMED CT core
    53563018 Acetyl-CoA: acyltransferase deficiency en Synonym Active Initial character case insensitive SNOMED CT core
    53564012 3-Ketothiolase deficiency en Synonym Active Case sensitive SNOMED CT core
    53565013 alpha-Methylacetoacetic aciduria en Synonym Active Case sensitive SNOMED CT core
    53566014 3-Methylhydroxybutyric acidemia en Synonym Active Case sensitive SNOMED CT core
    763292014 Acetyl-CoA: acyltransferase 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
    Acetyl-CoA: acyltransferase deficiency Is a Acidaemia false Inferred relationship Some
    Acetyl-CoA: acyltransferase deficiency Is a Non-amino organic acidaemia AND/OR aciduria false Inferred relationship Some
    Acetyl-CoA: acyltransferase deficiency Is a Enzymopathy false Inferred relationship Some
    Acetyl-CoA: acyltransferase deficiency Is a Autosomal recessive hereditary disorder false Inferred relationship Some
    Acetyl-CoA: acyltransferase deficiency Is a Inborn error of metabolism false Inferred relationship Some
    Acetyl-CoA: acyltransferase deficiency Occurrence Congenital false Inferred relationship Some
    Acetyl-CoA: acyltransferase deficiency Finding site Body system structure false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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