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191178002: Hemolytic anemia due to pyruvate kinase deficiency (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    294000010 Haemolytic anaemia due to pyruvate kinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    294001014 Hemolytic anemia due to pyruvate kinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    574846010 Hemolytic anemia due to pyruvate kinase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    294000010 Haemolytic anaemia due to pyruvate kinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    294000010 Haemolytic anaemia due to pyruvate kinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    294001014 Hemolytic anemia due to pyruvate kinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    294001014 Hemolytic anemia due to pyruvate kinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    574846010 Hemolytic anemia due to pyruvate kinase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    574846010 Hemolytic anemia due to pyruvate kinase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3454411001000118 Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    3454411001000118 Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Is a Hereditary hemolytic anemia false Inferred relationship Existential restriction modifier (core metadata concept)
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept) 4
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Associated etiologic finding Deficiency of pyruvate kinase false Inferred relationship Existential restriction modifier (core metadata concept)
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Due to Deficiency of pyruvate kinase false Inferred relationship Existential restriction modifier (core metadata concept) 5
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Has definitional manifestation Hemolysis false Inferred relationship Existential restriction modifier (core metadata concept)
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Interprets Red blood cell count false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Interprets Measurement of total haemoglobin concentration false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Interprets Erythrocyte destruction false Inferred relationship Existential restriction modifier (core metadata concept)
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Has interpretation Present (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Interprets Haemolysis false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Is a Anemia due to enzymopathy (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    SAME AS association reference set (foundation metadata concept)

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